Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Sexually Transmitted Infections from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 16
- Active, not recruiting: 11
- Completed: 13
- Other: 10
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00001316 — Viral Load in Blood and Lymph Tissues in People Living With HIV
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 400 |
| Study Type | OBSERVATIONAL |
| Conditions | HIV |
This is a study to determine the effect of the human immunodeficiency virus (HIV) on lymphoid tissues (e.g., lymph nodes) as compared to peripheral white blood cells. We have shown in previous studies that the lymph node is a major site of accumulation of HIV in the body, as well as being a site where much of the viral replication occurs which leads to the destruction of the body’s immune syste…
NCT00006518 — Specimen Collections From Participants With HIV Infection, KSHV Infection, Viral-Related Pre-malignant Lesions and Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1029 |
| Study Type | OBSERVATIONAL |
| Conditions | HIV; Kaposi’s Sarcoma; Lymphomas; Multicentric Castleman’s Disease; Primary Effusion Lymphoma |
BACKGROUND:
- A number of important scientific advances can be made through the study of blood, bone marrow, tumor, or other tissue samples from patients with HIV infection, infection with Kaposi s sarcoma associated herpesvirus (KSHV), infection with other oncogenic viruses, or cancer.
- This protocol provides a mechanism to affect a variety of such studies.
OBJECTIVES:
-Acquisition of seru…
NCT00029445 — Leukapheresis to Obtain Plasma or Lymphocytes for Studies of HIV-infected Patients, Including Long-term Non-progressors
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 400 |
| Study Type | OBSERVATIONAL |
| Conditions | HIV |
This study will collect white blood cells and plasma for research on how the immune system controls HIV infection. The immune system of a very small group of people with HIV, called non-progressors, has been able to control HIV for long periods without antiretroviral therapy. Some immune system-related genes important for this control have been identified in these patients.
People living with …
NCT01875588 — Thinking and Memory Problems in People With HIV
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 1150 |
| Study Type | OBSERVATIONAL |
| Conditions | HIV Positive |
Background:
- People with human immunodeficiency virus (HIV) can sometimes develop thinking and memory problems. These problems can vary widely, from few symptoms to severe problems with memory and concentration. It initially was thought that good HIV treatment could prevent almost all HIV-related memory problems. However, even people with low HIV viral loads can have these problems. It may b…
NCT04375800 — Doravirine (DOR) in Human Immunodeficiency Virus (HIV)-Infected Children Aged 4 Weeks to <12 Years and <45 kg (MK-1439-066)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Merck Sharp & Dohme LLC |
| Enrollment | 84 |
| Study Type | INTERVENTIONAL |
| Conditions | Human Immunodeficiency Virus (HIV) Infection |
| Interventions | ; ; |
This is a single-group, open-label, multi-site study in pediatric participants with human immunodeficiency virus type 1 (HIV-1) infection, aged 4 weeks to <12 years and weighing <45 kg, who are treatment-naive (TN) or have been virologically suppressed (VS) on stable combination antiretroviral therapy (cART) for ≥3 months with no history of treatment failure. The primary objectives are:
- To…
NCT04902443 — Pomalidomide and Nivolumab in People With Virus-Associated Malignancies With or Without HIV
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 58 |
| Study Type | INTERVENTIONAL |
| Conditions | Viral Associated Malignancies; Kaposi Sarcoma; EBV/KSHV-associated Lymphomas |
| Interventions | ; |
Background:
Less toxic and more effective treatments are needed for cancers caused by viruses. These cancers include Hodgkin and non-Hodgkin lymphoma, hepatocellular carcinoma, head and neck cancer, nasopharyngeal carcinoma, gastric cancer, anal cancer, cervical cancer, vaginal cancer, vulvar cancer, penile cancer, Merkel cell carcinoma, Kaposi sarcoma, and leiomyosarcoma. Researchers want to …
NCT05470491 — Trial of Allogeneic Reduced-Intensity, HLA-Haploidentical Allogeneic Hematopoietic Cell Bone Marrow Transplantation Followed by Graft-versus-Host-Disease (GVHD) Prophylaxis With Cyclophosphamide, Bortezomib and Maraviroc for Hematologic Malignancies …
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 265 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV; Hematologic Malignancies |
| Interventions | ; ; |
Background:
People living with HIV(PLWH) are at a higher risk for cancers that may be curable with a bone marrow transplant. HIV infection itself is no longer a reason to not get a transplant, for patients who otherwise have a standard reason to need transplant.
Objective:
This study is being done to see if a new combination of drugs (cyclophosphamide, maraviroc, and bortezomib) is both safe…
NCT06829602 — The Feasibility of Implementing Syphilis Point-of-care Testing Into a Prenatal Clinic for People Facing Barriers to Care
| Status | Recruiting |
| Phase | N/A |
| Sponsor | McMaster University |
| Enrollment | 77 |
| Study Type | INTERVENTIONAL |
| Conditions | Syphilis |
| Interventions |
The goal of this clinical trial is to learn if a finger-prick blood test for rapid diagnosis of syphilis infection can be implemented in a low-barrier prenatal clinic for people at risk of syphilis in pregnancy. The test gives results in 5 minutes and also tests for HIV.
The main questions the study aims to answer are:
- How often do pregnant people at risk of syphilis agree to the rapid test…
NCT07044297 — A Clinical Study of MK-8527 to Prevent Human Immunodeficiency Virus Type 1 (HIV-1) (MK-8527-011)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Merck Sharp & Dohme LLC |
| Enrollment | 4390 |
| Study Type | INTERVENTIONAL |
| Conditions | Human Immunodeficiency Virus (HIV); HIV Pre-Exposure Prophylaxis |
| Interventions | ; ; |
Researchers are looking for new medicines to prevent HIV-1 (Human Immunodeficiency Virus Type 1) infection.
The goals of this study are to learn:
- If taking MK-8527 once a month works to prevent HIV-1 infection as well as or better than a standard (usual) pre-exposure prophylaxis (PrEP) taken once a day
- About the safety of MK-8527 and if people tolerate it
NCT07281430 — Self-collection for HPV Testing to Improve Cervical Cancer Prevention (SHIP) Trial (LMI-001-A-S04)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 500 |
| Study Type | INTERVENTIONAL |
| Conditions | Cervical Carcinoma; Human Papillomavirus Infection |
| Interventions | ; ; |
This clinical trial evaluates the use of self-collected vaginal samples for human papillomavirus (HPV) testing in patients referred for a colposcopy and/or cervical excisional procedures to improve cervical cancer prevention. HPV is a common virus which usually causes infections that last only a few months, but sometimes can last longer. HPV is known to cause a variety of cancers including cerv…
NCT06389565 — Change My Story Task Shifted Mental Health Intervention
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Massachusetts General Hospital |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Hiv; Depression; Psychological Distress |
| Interventions | ; |
Psychological distress and depression are common among young people living with HIV (Y-PLWH) and negatively impact medication adherence and disease control. In low- and middle-income countries, this problem is compounded by the lack of trained mental health professionals on the provider side and the requirement of frequent clinic-based visits imposing greater cost, inconvenience, and stigma for…
NCT06819176 — Lenacapavir Intensification to Disrupt HIV Reservoirs in Virologically Suppressed People With HIV Receiving Antiretroviral Therapy
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Human Immunodeficiency Virus |
| Interventions |
Background:
Antiretroviral viral therapy (ART) allows people with human immunodeficiency (HIV) to live long, healthy lives. But ART is not a cure. HIV can remain in the body, in infected cells called reservoirs. If a person stops taking ART, the HIV can rebound and reach high levels in their blood. Researchers want to find ways to reduce the size of HIV reservoirs in people taking ART.
Object…
NCT06797986 — A Phase I/IIa Clinical Trial to Investigate BVAC-E6E7 in Subjects With HPV Positive HNSCC.
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Cellid Co., Ltd. |
| Enrollment | 37 |
| Study Type | INTERVENTIONAL |
| Conditions | Head and Neck Squamous Cell Carcinoma (HNSCC); HPV (Human Papillomavirus)-Associated Carcinoma; HPV Positive Oropharyngeal Squamous Cell Carcinoma |
| Interventions | ; ; |
BVAC-E6E7 is an immunotherapeutic vaccine designed to treat unresectable recurrent or metastatic head and neck squamous cell carcinoma positive to HPV 16 or 18. This clinical trial for BVAC-E6E7 consists of two phases: PhaseⅠfocuses on safety and tolerance to determine the maximum tolerated dose (MTD), while Phase Ⅱ evaluates its efficacy.
NCT07342491 — Dasatinib for HIV-1 Reservoir Reduction
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 14 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV Infections |
| Interventions | ; |
This study will test if the medicine dasatinib can lower the hidden amount of HIV in the body, called the HIV “reservoir.” It will also check if dasatinib is safe and easy to take for people living with HIV who have a suppressed viral load while on antiretroviral therapy (ART). Adults 18 years or older who have been on ART for at least 48 months and have had a suppressed HIV-1 viral load for at…
NCT07458802 — Healthy Expectancy Through Routine Antenatal STI Screening
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Adriane Wynn |
| Enrollment | 2000 |
| Study Type | INTERVENTIONAL |
| Conditions | Antenatal Health; Antenatal Care; STI; Chlamydia Trachomatis Infection in Pregnancy; Chlamydia |
| Interventions |
This study will evaluate whether routine screening and treatment for two common sexually transmitted infections, chlamydia and gonorrhoea, during pregnancy can reduce preterm birth and other poor birth outcomes in Botswana, and whether this approach is affordable and cost-effective for the health system.
About 2,000 pregnant women attending their first antenatal care visit at up to 10 governme…
NCT07636928 — Mass Balance and Absolute Oral Bioavailability of [14C]VH4524184
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | ViiV Healthcare |
| Enrollment | 9 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV Infections |
| Interventions | ; ; |
The purpose of the study is to assess the bioavailability, mass balance, pharmacokinetics, metabolism and excretion of radiolabeled (14C) VH4524184.
Active, Not Recruiting
NCT00092222 — Virotherapy and Natural History Study of KHSV-Associated Multricentric Castleman s Disease With Correlates of Disease Activity
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 75 |
| Study Type | INTERVENTIONAL |
| Conditions | Lymphoproliferative Disorder; HHV-8; Malignancy; HIV |
| Interventions | ; ; |
This study will gain information about a rare disorder called KSHV-associated multicentric Castleman’s disease (MCD). KSHV, a virus, causes several kinds of cancer, including some forms of MCD. KSHV stands for the Kaposi’s sarcoma herpes virus, also called human herpes virus-8, or HHV-8. Researchers want to understand the biology of KSHV-MCD to identify how this disease causes illness and to fi…
NCT00867464 — Extended Follow Up of Young Women in Costa Rica Who Received Vaccine for Human Papillomavirus Types 16 and 18 and Unvaccinated Controls
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 8670 |
| Study Type | OBSERVATIONAL |
| Conditions | Anal Carcinoma; Cervical Carcinoma; Human Papillomavirus Infection; Human Papillomavirus-Related Cervical Carcinoma; Oral Cavity Carcinoma |
| Interventions | ; ; |
This research trial studies extended follow up of young women in Costa Rica who received vaccine for human papillomavirus types 16 and 18 and unvaccinated controls. Collecting information from young women in Costa Rica who have received vaccine for human papillomavirus types 16 and 18 and a new group of unvaccinated controls enrolled for the follow-up period, may help doctors learn more about t…
NCT02816879 — Anal Cytology Collection Procedures in Predicting High-Grade Anal Dysplasia in Men Who Have Sex With Men
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Jonsson Comprehensive Cancer Center |
| Enrollment | 415 |
| Study Type | INTERVENTIONAL |
| Conditions | Anal Carcinoma; HIV Infection; Human Papillomavirus Infection |
| Interventions | ; |
This clinical trial compares three anal cytology collection procedures (collected at a single visit) in men who have sex with men (MSM). It also compares two different tests for human papilloma virus, the virus that causes high grade anal dysplasia, which is thought to occur before anal cancer. This study may help doctors develop better screening for high-grade anal dysplasia in MSM in order to…
NCT02494986 — A Roll-over Study With Rilpivirine for Human Immunodeficiency Virus Type 1 (HIV-1) Infected Participants Who Participated in Rilpivirine Pediatric Studies
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Janssen Sciences Ireland UC |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Human Immunodeficiency Virus Type 1 |
| Interventions |
The purpose of this study is to provide continued access to rilpivirine (RPV) for participants who were treated with RPV in a clinical development pediatric study with rilpivirine and who, at the time of roll-over, experience and are expected to continue experiencing clinical benefit from RPV treatment.
NCT02951052 — Study Evaluating the Efficacy, Safety, and Tolerability of Switching to Long-acting Cabotegravir Plus Long-acting Rilpivirine From Current Antiretroviral Regimen in Virologically Suppressed HIV-1-infected Adults
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | ViiV Healthcare |
| Enrollment | 618 |
| Study Type | INTERVENTIONAL |
| Conditions | Infection, Human Immunodeficiency Virus; HIV Infections |
| Interventions | ; ; |
The Antiretroviral Therapy as Long Acting Suppression (ATLAS) study is being conducted to establish if human immunodeficiency virus type-1 (HIV-1) infected adult subjects with current viral suppression on a regimen with 2 nucleoside reverse transcriptase inhibitors (NRTIs) plus a third agent, remain suppressed upon switching to a two-drug intramuscular (IM) long-acting (LA) regimen of cabotegra…
NCT03296202 — Risk of Morbidity, Mortality and Long-term Monitoring of Antiretroviral Treatment in People Living With HIV
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Bordeaux |
| Enrollment | 7500 |
| Study Type | OBSERVATIONAL |
| Conditions | HIV Infections; Antiretroviral Agents |
HIV infection is now a chronic disease in countries where antiretroviral treatments (ART) are largely available. Long-term follow-up is required to describe and understand the evolution of morbidities and complications as well as new treatments side effects.
The main objective of the cohort is to describe and study the evolution of HIV infection in ART-treated individuals.
NCT05979311 — A Study to Evaluate the Efficacy, Safety, and Tolerability of Using an Oral Once-daily 2 Drug Regimen Compared to an Oral Once-daily 3 Drug Regimen for the Treatment of Human Immunodeficiency Virus (HIV)-1 in Adults Who Have Not Previously Taken Antiretroviral Therapy
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | ViiV Healthcare |
| Enrollment | 307 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV; HIV Infections |
| Interventions | ; ; |
This study will compare safety, efficacy, participant reported outcomes and implementation outcomes of a fixed dose combination (FDC) of a two-drug regimen dolutegravir (DTG) plus lamivudine (3TC) and a three-drug regimen FDC of bictegravir (BIC), emtricitabine (FTC) and tenofovir alafenamide (TAF) in HIV-1 infected adult participants who have not previously received antiretroviral therapy.
NCT06611540 — Self-collection for HPV Testing to Improve Cervical Cancer Prevention (SHIP) Trial (LMI-001-A-S03)
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 500 |
| Study Type | INTERVENTIONAL |
| Conditions | Cervical Carcinoma; Human Papillomavirus Infection |
| Interventions | ; ; |
This clinical trial evaluates the use of self-collected vaginal samples for human papillomavirus (HPV) testing in patients referred for a colposcopy and/or cervical excisional procedures to improve cervical cancer prevention. HPV is a common virus which usually causes infections that last only a few months, but sometimes can last longer. HPV is known to cause a variety of cancers including cerv…
NCT06611553 — Self-collection for HPV Testing to Improve Cervical Cancer Prevention (SHIP) Trial (LMI-001-A-S02)
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 500 |
| Study Type | INTERVENTIONAL |
| Conditions | Cervical Carcinoma; Human Papillomavirus Infection |
| Interventions | ; ; |
This clinical trial evaluates the use of self-collected vaginal samples for human papillomavirus (HPV) testing in patients referred for a colposcopy and/or cervical excisional procedures to improve cervical cancer prevention. HPV is a common virus which usually causes infections that last only a few months, but sometimes can last longer. It is known to cause a variety of cancers including cance…
NCT06497504 — Study of Bepirovirsen in Participants Living With Human Immunodeficiency Virus and Chronic Hepatitis B Virus Infection (B-Focus)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | GlaxoSmithKline |
| Enrollment | 153 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatitis B |
| Interventions | ; |
This study will evaluate the efficacy and safety of bepirovirsen compared to placebo in participants with human immunodeficiency virus (HIV)/hepatitis B virus (HBV) co-infection.
NCT07053384 — A Study to Investigate the Use of VH3810109 With or Without Fostemsavir (FTR) to Reduce the Size and Activity of the Viral Reservoir in People Living With HIV
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | ViiV Healthcare |
| Enrollment | 130 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV Infections |
| Interventions | ; ; |
This study investigates the use of VH3810109 with or without FTR to reduce the size and activity of the HIV viral reservoir in two sub-populations of people living with HIV: treatment-naïve adults (Population 1) and treatment-experienced adults currently taking a standard of care (SOC) integrase strand transfer inhibitor (INSTI)-based antiretroviral therapy (ART) regimen (Population 2). The stu…
Not Yet Recruiting
NCT07681908 — #TranscendentHealth: A Text Messaging Pregnancy Prevention Program for Transgender Boys
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Center for Innovative Public Health Research |
| Enrollment | 467 |
| Study Type | INTERVENTIONAL |
| Conditions | Pregnancy (Unwanted); Sexually Transmitted Disease (STD); HIV Infection; Sexual Behavior |
| Interventions | ; |
Transgender and gender-diverse young people who were assigned female at birth (AFAB), including transgender boys, nonbinary youth, and others, face real sexual health disparities. Existing pregnancy and HIV prevention programs are designed for cisgender girls and do not meet the needs of AFAB trans youth, leaving this group without programs that speak to their lives.
#TranscendentHealth is a t…
NCT07620652 — Pilot Study to Evaluate Efficacy and Safety of Switching to BIC/FTC/TAF in PWH With a Previous Virological Failure Under CAB/RPV LAI
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Cristina Mussini |
| Enrollment | 30 |
| Study Type | OBSERVATIONAL |
| Conditions | HIV Infection |
This study is a pilot, multi-center, observational retrospective-prospective study, with two different Parts, as follows:
- Part 1(retrospective and prospective part): to evaluate efficacy and safety of switching to BIC/FTC/TAF in People living with HIV (PWH) who previously failed CAB/RPV LAI in the last three years and received in the last three years boosted PI since any INSTI mutations wer…
NCT07682961 — Study of Lenacapavir, Teropavimab, and Zinlirvimab Versus Cabotegravir and Rilpivirine in Virologically Suppressed Adults With HIV-1 on Oral Daily Antiretroviral Therapy
| Status | Not yet recruiting |
| Phase | Phase 3 |
| Sponsor | Gilead Sciences |
| Enrollment | 590 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV Infections |
| Interventions | ; ; |
The goal of this clinical study is to compare how effective a long-acting injectable treatment of lenacapavir (LEN), teropavimab (TAB), and zinlirvimab (ZAB) versus (CAB) and rilpivirine (RPV) injections given every 8 weeks in adults with HIV-1 whose virus is well controlled on daily oral treatment, after 1 year (52 weeks) of the treatment.
The primary objective of this study are to evaluate t…
NCT07669363 — Hexaminolevulinate Photodynamic Therapy (HAL-PDT) With Deferred Surgery Versus Surgery for High-grade Squamous Intraepithelial Lesions (HSIL)
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University |
| Enrollment | 230 |
| Study Type | INTERVENTIONAL |
| Conditions | Cervical Intraepithelial Neoplasia; Papillomavirus Infections |
| Interventions | ; |
High-grade squamous intraepithelial lesions (HSIL), encompassing cervical intraepithelial neoplasia grade 2 (CIN2) with p16 positivity and grade 3 (CIN3), are precancerous conditions that require effective intervention. This Phase II study aims to comprehensively evaluate the efficacy, safety, and impact on quality of life of hexaminolevulinate photodynamic therapy (HAL-PDT) with deferred surge…
NCT06810739 — The Women’s Screening and Self-Testing Program (PROMETA) Study
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Tulane University |
| Enrollment | 8445 |
| Study Type | INTERVENTIONAL |
| Conditions | Human Papilloma Virus Related Cervical Carcinoma |
| Interventions |
This proposal directly addresses the ability to safely scale-up a Screen-Triage-Treat approach to cervical cancer screening. The investigators propose to capitalize on a pool of screen-eligible women accessing routine care within targeted human immunodeficiency virus (HIV) care and treatment services. The primary outcome of interest is the number of women screened and the proportion of screen-p…
NCT07691424 — Impact of Migration History and Social Conditions on the Immuno-virological Control of HIV in Migrants in France
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Clermont-Ferrand |
| Enrollment | 150 |
| Study Type | OBSERVATIONAL |
| Conditions | HIV - Human Immunodeficiency Virus; Socio-economic Status; Migrants |
Migrants living with HIV - whether the infection was diagnosed in their country of origin or in France- frequently experience vulnerabilities related to their migration trajectories and often face socioeconomic and administrative instability upon arrival .
The primary outcome of this study is to compare the immunovirological efficacy of antiretroviral therapy among migrants living with HIV pat…
NCT07600775 — A Clinical Trial of MK-8527 and Rifampin in Adult Participants With Latent Tuberculosis Infection (MK-8527-019)
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | Merck Sharp & Dohme LLC |
| Enrollment | 14 |
| Study Type | INTERVENTIONAL |
| Conditions | Human Immunodeficiency Virus (HIV); HIV Pre-Exposure Prophylaxis |
| Interventions | ; |
Researchers are studying MK-8527, a new medicine for preventing HIV-1 (human immunodeficiency virus type 1) infection and want to learn if MK-8527 can be given together with rifampin. Rifampin is commonly used to treat people with latent tuberculosis infection (LTBI).
The main goal of this study is to learn what happens to MK-8527 in the body over time when given with and without the medicatio…
NCT07578467 — Combining Neo-adjuvant ATR-inhibition With Nodal SBRT for Early-stage Resectable HPV+ OPSCCs
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Abramson Cancer Center at Penn Medicine |
| Enrollment | 35 |
| Study Type | INTERVENTIONAL |
| Conditions | HPV Positive Oropharyngeal Squamous Cell Carcinoma; Squamous Cell Carcinoma; HPV (Human Papillomavirus)-Associated Carcinoma; HPV Associated Cancers; Oropharyngeal HPV Squamous Cell Carcinoma |
| Interventions | ; |
This research study is testing whether a new study drug (called ATRN-119) is safe and effective when combined with a single, highly targeted dose of radiation therapy (called stereotactic body radiation therapy or SBRT) to treat early-stage throat cancer that is caused by HPV.
The goal of this study is to treat cancer effectively while reducing side effects and helping patients maintain a bett…
NCT07667127 — Comparing Digital and Collaborative Gamified Reinforcement Strategies for HPV Literacy and Retention Among Nursing Students
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Aydin Adnan Menderes University |
| Enrollment | 64 |
| Study Type | INTERVENTIONAL |
| Conditions | Health Literacy; Human Papillomavirus (HPV) Infection; Nursing Education |
| Interventions | ; |
This randomized comparative study aims to evaluate the effectiveness of two gamified reinforcement strategies, Gimkit and Escape Room, on human papillomavirus (HPV) literacy, short-term retention, and gameful learning experiences among undergraduate nursing students. Following standardized theoretical instruction on HPV infection, participants will be randomly assigned to either a digital quiz-…
NCT06015581 — Scaling Up Implementation Strategies to Improve the DIAGNOSE and PREVENT Pillars for Young MSM in Florida
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Florida State University |
| Enrollment | 81 |
| Study Type | INTERVENTIONAL |
| Conditions | Hiv |
| Interventions | ; |
The purpose of this study is to evaluate the Young Adult Centered HealthForce Training (YACHT) package in 41 Florida Department of Health (FDOH) contracted Counseling, Testing, and Referral (CTR) agencies across six Florida End the Epidemic (EHE) counties. Agencies will be cluster-stratified and randomized to either the YACHT intervention (20 agencies) or a comparison group (21 agencies). The p…
Completed Trials
NCT00001393 — Genetic Markers for Focal Segmental Glomerulosclerosis
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Enrollment | 616 |
| Study Type | OBSERVATIONAL |
| Conditions | Focal Segmental Glomerulosclerosis; HIV-Associated Focal Segmental Glomerulosclerosis |
Glomerulonephritis is a disease which affect the kidneys. Occasionally these diseases can progress to a loss of kidney function in some patients. Glomerulosclerosis or focal segmental glomerulosclerosis (FSGS) is one form of glomerulonephritis.
The cause of FSGS is unknown and often occurs on its own (idiopathic), or it can be associated with HIV (Human Immunodeficiency Virus). FSGS occurs mor…
NCT02344680 — Liver Fibrosis in Zambian HIV-HBV Co-infected Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 349 |
| Study Type | OBSERVATIONAL |
| Conditions | Human Immunodeficiency Virus; HBV; Fibrosis, Liver; Cirrhosis, Liver; Hepatocellular Carcinoma |
| Interventions |
A cohort of adults with HIV-HBV co-infection will be created in Lusaka, Zambia, to describe the short and long-term (up to 10 years of follow-up) HBV and liver outcomes, including the effectiveness of current therapies, and to identify the risk factors for major endpoints of interest, including HCC and HBV functional cure. This cohort will also create a pool of potential participants for in-dep…
NCT03603808 — VGX-3100 and Electroporation in Treating Patients With HIV-Positive High-Grade Anal Lesions
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | AIDS Malignancy Consortium |
| Enrollment | 44 |
| Study Type | INTERVENTIONAL |
| Conditions | Anal Intraepithelial Neoplasia; High Grade Squamous Intraepithelial Neoplasia; HIV Positivity; Human Papillomavirus-16 Positive; Human Papillomavirus-18 Positive |
| Interventions | ; ; |
This phase II trial studies the use of human papillomavirus (HPV) deoxyribonucleic acid (DNA) plasmids therapeutic vaccine VGX-3100 (VGX-3100) and electroporation in treating patients with human immunodeficiency virus (HIV)-positive high-grade anal lesions. Vaccines made from DNA may help the body build an effective immune response to kill tumor cells. Electroporation helps pores in your body’s…
NCT03600142 — A Stigma Reduction Intervention at Time of Entry Into Antenatal Care to Improve PMTCT Services in Tanzania
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Utah |
| Enrollment | 1539 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV Infections |
| Interventions |
This study will pilot test a brief, scalable intervention called Maisha (Swahili for life), to address HIV stigma for women presenting to antenatal care in Tanzania and male partners who accompany them. The intervention will include: 1) a video and brief counseling that addresses HIV stigma at the start of the ANC visit (prior to HIV testing), and 2) two stigma-based counseling sessions for ind…
NCT03733093 — PREVAIL VIII: A CoHOrt Clinical, Viral, and ImmuNOlogic Monitoring Study of People Living With Retroviral Infection in Liberia (HONOR)
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 1377 |
| Study Type | OBSERVATIONAL |
| Conditions | HIV |
Background:
There are many people living with human immunodeficiency virus (HIV) infection in Liberia. Most experts consider HIV an epidemic there. Researchers want to collect health data from Liberians with HIV over several years. This may help HIV prevention and treatment programs in Liberia.
Objective:
To learn more about how HIV affects people in Liberia.
Eligibility:
People with HIV i…
NCT05069974 — Alternative Antibiotics for Syphilis
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia |
| Enrollment | 224 |
| Study Type | INTERVENTIONAL |
| Conditions | Early Latent Syphilis; Primary Syphilis; Secondary Syphilis |
| Interventions | ; |
The Trep-AB clinical trial will test the efficacy of an investigational neuropenetrative drug, Linezolid (LZD), compared to standard treatment, Benzathine penicillin G (BPG), for early syphilis in humans. The overarching idea of the work proposed herein is to investigate the use of LZD to treat syphilis, conducting a randomized controlled clinical trial to evaluate this new indication of a know…
NCT05040841 — Supporting Sustained HIV Treatment Adherence After Initiation
| Status | Completed |
| Phase | N/A |
| Sponsor | Boston University |
| Enrollment | 534 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV Infections; Adherence, Medication |
| Interventions | ; ; |
The investigators will implement a 24-month fractional factorial design study (Aim 1). The investigators will recruit 510 patients initiating antiretroviral therapy (ART) at three City of Cape Town ART clinics. Each patient will have adherence monitored using the Wisepill® electronic adherence monitoring device (EAM). After eligibility has been confirmed, each participant will be randomized to …
NCT04265950 — Establishing Optimal Number of Doses for HPV Vaccination in Children and Adolescents Living With HIV, OPTIMO Trial
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Fred Hutchinson Cancer Center |
| Enrollment | 97 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV Infection |
| Interventions |
This phase IV trial compares 3 different dosing schedules to find the optimal number of doses for HPV vaccination in children and adolescents living with HIV. Comparing 3 different dosing schedules may help researchers determine whether a single dose of HPV vaccine could be effective in preventing HPV in children and adolescents living with HIV.
NCT04868123 — Effects of TENS and Mindfulness Meditation in Persons With HIV-related Neuropathy
| Status | Completed |
| Phase | N/A |
| Sponsor | Rutgers University |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV Infections |
| Interventions | ; |
This study is to explore the effects of transcutaneous nerve stimulation (TENS) and mindfulness meditation in persons living with HIV (PLHIV) and painful neuropathy in the feet.
NCT05405582 — Thetha Nami Ngithethe Nawe (“Let’s Talk”): Step Wedge cRCT of Peer Led Community PrEP and SRH for Youth in South Africa
| Status | Completed |
| Phase | N/A |
| Sponsor | Africa Health Research Institute |
| Enrollment | 8716 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV-1-infection; Sexually Transmitted Diseases |
| Interventions | ; |
Study Hypothesis: Social mobilisation will attract and engage young people into decentralised sexual reproductive health (SRH) services where HIV prevention is tailored to need. Decentralised risk informed (differentiated) biosocial HIV prevention will reduce the overall prevalence of sexually transmissible HIV amongst young people aged 15-30.
Study aims:
- Measure the impact of social mobil…
NCT06302725 — Vaginal Self-sampling for Detecting High-risk Human Papillomavirus Cervical Infection in Patients With Immune-mediated Inflammatory Diseases
| Status | Completed |
| Phase | N/A |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Enrollment | 278 |
| Study Type | INTERVENTIONAL |
| Conditions | HPV Infection; Systemic Disease |
| Interventions |
Main objective: -To determine Human Papilloma Virus (HPV) prevalence in patients with immune-mediated inflammatory diseases (IMID) using vaginal self-sampling (VSS), one year after VSS was proposed Primary endpoint: - To determine the prevalence of HPV infection (yes/no) after VSS proposal Secondary objectives: - To describe the HPV typology and the rate of co-infection (with several high-risk …
NCT05335096 — An AI-based mHealth Intervention to Improve HIV Testing
| Status | Completed |
| Phase | N/A |
| Sponsor | Yale University |
| Enrollment | 307 |
| Study Type | INTERVENTIONAL |
| Conditions | HIV Infections |
| Interventions | ; ; |
The purpose of this study is to develop an artificial intelligence (AI)-chatbot-based mobile health (mHealth) intervention to promote HIV testing in Malaysia.
NCT07557719 — Gamified Learning Methods and HPV Knowledge in Nursing Students
| Status | Completed |
| Phase | N/A |
| Sponsor | Aydin Adnan Menderes University |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Game-Based Learning; Educational Intervention; Nursing Education |
| Interventions | ; |
This study is a randomized controlled trial (RCT) with a pretest-posttest-follow-up design that compares the effectiveness of gamified teaching methods (Gimkit and educational escape room) with traditional theoretical education in improving undergraduate nursing students’ Human Papillomavirus (HPV) knowledge and HPV literacy. Both HPV knowledge and HPV literacy were prespecified primary outcome…