Clinical Trials for Infectious Diseases

Currently registered clinical trials for Infectious Diseases from ClinicalTrials.gov. 23 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

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 Infectious Diseases from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 23
  • Active, not recruiting: 3
  • Completed: 16
  • Other: 8

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT00001281 — Studies of the Pathogenesis of HIV Infection in Human Peripheral Blood Cells and/or Body Fluids in People Living With and Without HIV

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment2419
Study TypeOBSERVATIONAL
ConditionsHIV; Immunodeficiencies; Infectious Diseases

We are studying virologic and/or immunologic parameters of HIV infection and other infectious or non-infectious immune deficiency diseases in order to better understand the pathogenesis of HIV. Because of the lack of an adequate animal model it is generally necessary to utilize human peripheral blood cells for studying aspects of either in vivo or in vitro HIV infection. We wish to be able to c…

NCT00001352 — Fungal Infection Susceptibility

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment800
Study TypeOBSERVATIONAL
ConditionsCryptococcal Infection; Cryptococcal Pneumonia; Pulmonary Cryptococcosis; Cryptococcal Meningitis; Cryptococcosis

The protocol will be carried out in accordance with International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Good Clinical Practice (GCP) and the following United States Code of Federal Regulations (CFR) applicable to clinical studies: 45 CFR Part 46, 21 CFR Part 50, 21 CFR Part 56, 21 CFR Part 312, and/or 21 CFR Part 812.

NIH-funded investigato…

NCT00001778 — Evaluation of Patients With HAM/TSP

StatusRecruiting
PhaseN/A
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment750
Study TypeOBSERVATIONAL
ConditionsHTLV-I Infection; Tropical Spastic Paraparesis

Objective:

Human T-lymphotropic virus type-I-associated myelopathy / tropical spastic paraparesis (HAM/TSP) is a rare neurologic disorder that affects less than 5% of patients infected with the HTLV-I virus. The purpose of this protocol is to study the natural history of HAM/TSP by monitoring clinical progression of patients longitudinally. Additionally, we will attempt to define the virologic…

NCT00006150 — Natural History, Management, and Genetics of the Hyperimmunoglobulin E Recurrent Infection Syndrome (HIES)

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment600
Study TypeOBSERVATIONAL
ConditionsInfections; Pneumonia; Immune System Diseases; STAT3 Transcription Factor; Job Syndrome

The Hyper IgE Syndromes (HIES) are primary immunodeficiencies resulting in eczema and recurrent skin and lung infections. Autosomal dominant Hyper IgE syndrome (AD-HIIES; Job’s syndrome) is caused by STAT3 mutations, and is a multi-system disorder with skeletal, vascular, and connective tissue manifestations. Understanding how STAT3 mutations cause these diverse clinical manifestations is criti…

StatusRecruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment1029
Study TypeOBSERVATIONAL
ConditionsHIV; 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

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment400
Study TypeOBSERVATIONAL
ConditionsHIV

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 …

NCT00077909 — Study of Lung Proteins in Patients With Pneumonia

StatusRecruiting
PhaseN/A
SponsorNational Institutes of Health Clinical Center (CC)
Enrollment750
Study TypeOBSERVATIONAL
ConditionsPneumonia; Pulmonary Disease; Lung Disease

This study will examine the different types of proteins present in the lungs of patients with pneumonia to explore the causes of different types of the disease. Pneumonia is a condition that causes lung inflammation AND is often caused by an infection. It is usually diagnosed by lung x-rays and listening to the chest with a stethoscope. This method can diagnose pneumonia, but it does not provid…

NCT00128973 — Evaluation of Patients With Immune Function Abnormalities

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment3500
Study TypeOBSERVATIONAL
ConditionsChronic Granulomatous Disease (CGD); X-Linked Severe Combined Immune Deficiency (XSCID); Leukocyte Adhesion Deficiency 1 (LAD); Graft Versus Host Disease (cGvHD)

This study will evaluate patients with abnormal immune function that results in recurrent or unusual infections or chronic inflammation. This may include inherited conditions, such as X-linked severe combined immunodeficiency (XSCID), chronic granulomatous disease (CGD), and leukocyte adhesion deficiency (LAD), or conditions resulting from outside factors, such as graft-versus-host disease (GVH…

NCT00404560 — Detection and Characterization of Infections and Infection Susceptibility

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment2000
Study TypeOBSERVATIONAL
ConditionsImmune Deficiencies

This screening study will examine the causes of immune disorders affecting white blood cells, which defend against infections and will try to develop better means of diagnosis and treatment of these immune disorders. This is a 2 visit screening study and patients determined to be of interest for additional study or treatment will be asked to provide consent for enrollment into an appropriate NI…

NCT00943514 — Natural History of Bronchiectasis

StatusRecruiting
PhaseN/A
SponsorNational Heart, Lung, and Blood Institute (NHLBI)
Enrollment900
Study TypeOBSERVATIONAL
ConditionsBronchiectasis; Cystic Fibrosis; Autoimmune Disease; Common Variable Immunodeficiency

Background:

  • Bronchiectasis is a disease characterized by airways that are inflamed, abnormally dilated, and chronically infected. Individuals with bronchiectasis have a history of chronic and recurring respiratory infections. Depending on the underlying cause, these infections may involve the entire respiratory tract, resulting in sinus, ear, and lung disease.
  • Bronchiectasis continues to b…

NCT01306084 — Viral Infections in Healthy and Immunocompromised Hosts

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsAnogenital Herpes; COVID-19; Herpes Labialis

Background:

- Viral infections are an important cause of illness and death in hospitalized patients as well as outpatients. New strains of viruses may appear and infect both healthy people and those with weak immune systems. A better understanding of these new virus strains (such as SARS-CoV-2, the virus that causes COVID-19) may help to control and prevent these infections. In particular, so…

NCT01386424 — Screening for LID Clinical Studies Unit Healthy Volunteer Protocols

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment5000
Study TypeOBSERVATIONAL
ConditionsZika; Influenza

Background:

  • The Laboratory of Infectious Diseases (LID) Clinical Studies Unit (CSU) enrolls healthy volunteers into clinical studies to study infectious diseases.
  • Viruses can be highly infectious and contagious. They cause considerable illness in the United States each year and a good example of this is influenza (the flu). The LID CSU performs clinical studies to learn about these viral i…

NCT01875588 — Thinking and Memory Problems in People With HIV

StatusRecruiting
PhaseN/A
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment1150
Study TypeOBSERVATIONAL
ConditionsHIV 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…

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment600
Study TypeOBSERVATIONAL
ConditionsGATA2 Deficiency

Background:

- GATA2 deficiency is a genetic disorder that can cause problems with a person s immune system and other body systems. Some people who have this disorder develop few problems from it. Others can have a wide range of health problems, from skin problems, to hearing loss, to cancer. These problems can happen at any age. Researchers want to study GATA2 deficiency to better understand …

NCT02435810 — Inflammatory and Infectious Diseases of the Nervous System

StatusRecruiting
PhaseN/A
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsBrain Disease

Background:

- Inflammation is how the body reacts to infection or injury. Infections or inflammation in the brain and nerves can be serious. There aren t always good tests to detect this. Researchers want to learn more about how diseases affect the brain and nerves to develop better tests and treatments.

Objective:

- To learn more about how inflammation and infections hurt the brain and ne…

NCT04902443 — Pomalidomide and Nivolumab in People With Virus-Associated Malignancies With or Without HIV

StatusRecruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment58
Study TypeINTERVENTIONAL
ConditionsViral 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 …

NCT04876131 — Single Dose Intravenous Antibiotics for Complicated Urinary Tract Infections in Children

StatusRecruiting
PhasePhase 4
SponsorMurdoch Childrens Research Institute
Enrollment452
Study TypeINTERVENTIONAL
ConditionsComplicated Urinary Tract Infection; Infection; Pediatric Infectious Disease
Interventions; ;

Urinary tract infections (UTI) are commonly encountered in children, with 7% diagnosed with at least one UTI by the age of 19 years. The evidence for treatment of uncomplicated UTI is clear; oral antibiotics are as good as intravenous (IV) antibiotics, usually for a total of 7 days. Complicated UTIs (cUTIs) on the other hand, are common reasons for hospital admissions for IV antibiotics and con…

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 …

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment265
Study TypeINTERVENTIONAL
ConditionsHIV; 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…

NCT06000761 — Frequent Standardized Oral Care Using Human Milk in the Neonatal Intensive Care Unit

StatusRecruiting
PhaseN/A
SponsorUniversity of Florida
Enrollment218
Study TypeINTERVENTIONAL
ConditionsVentilator Associated Pneumonia; Bronchopulmonary Dysplasia; Respiratory Disease
Interventions

Premature infants are susceptible to complications related to infrequent and non-standardized oral care. Although the benefits of frequent standardized oral care are known to reduce oral dysbiosis (increased level of potentially pathogenic bacteria) and its associated complications in critically ill adults leading to established evidence-based guidelines, no such information exists for VLBW inf…

NCT07069400 — An International Observational Study of Adults With Acute Infection

StatusRecruiting
PhaseN/A
SponsorUniversity of Minnesota
Enrollment1500
Study TypeOBSERVATIONAL
ConditionsInfectious Disease
Interventions

Prospective, longitudinal studies of people with acute infections are essential to understand risk factors, clinical manifestations, pathobiology, and management strategies. Observational studies can provide data necessary to select interventions and strategies for testing in clinical trials and to develop key design features of trials. Observational studies can be particularly important for es…

NCT06819176 — Lenacapavir Intensification to Disrupt HIV Reservoirs in Virologically Suppressed People With HIV Receiving Antiretroviral Therapy

StatusRecruiting
PhasePhase 1
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment50
Study TypeINTERVENTIONAL
ConditionsHuman 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.

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorCellid Co., Ltd.
Enrollment37
Study TypeINTERVENTIONAL
ConditionsHead 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.

NCT07406360 — A Study on the Immune Response and Safety of an Investigational Combined Measles, Mumps, Rubella and Varicella Vaccine, When Administered as Intramuscular Injection to Healthy Children 15 Months to 6 Years of Age

StatusRecruiting
PhasePhase 3
SponsorGlaxoSmithKline
Enrollment1209
Study TypeINTERVENTIONAL
ConditionsMeasles; Measles-Mumps-Rubella+Chickenpox Vaccine
Interventions;

This study is evaluating the immunogenicity and safety of intramuscular administration of the investigational MMRVNS vaccine compared to intramuscular administration of the MMRV (Merck’s measles, mumps, rubella and varicella) vaccine (ProQuad) that is already licensed for this route, when administered as a second dose in children 15 months to 6 years of age who were previously primed with a fir…

Active, Not Recruiting

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

StatusActive, not recruiting
PhasePhase 3
SponsorViiV Healthcare
Enrollment618
Study TypeINTERVENTIONAL
ConditionsInfection, 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…

NCT06497504 — Study of Bepirovirsen in Participants Living With Human Immunodeficiency Virus and Chronic Hepatitis B Virus Infection (B-Focus)

StatusActive, not recruiting
PhasePhase 2
SponsorGlaxoSmithKline
Enrollment153
Study TypeINTERVENTIONAL
ConditionsHepatitis 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.

NCT07690956 — Pharmacist-Led Education to Improve Neutropenic Precautions in Cancer Patients

StatusActive, not recruiting
PhaseN/A
SponsorJordan University of Science and Technology
Enrollment300
Study TypeINTERVENTIONAL
ConditionsFebrile Neutropenia
Interventions

The goal of this clinical trial is to test whether pharmacist-led education can improve knowledge and adherence to neutropenic precautions and reduce infection rates in adult cancer patients receiving high-risk chemotherapy. The main questions it aims to answer are:

  • Does pharmacist-led education improve patient knowledge of neutropenic fever prevention?
  • Does it increase adherence to precau…

Not Yet Recruiting

NCT07643974 — Coupled Gentamicin-Lactobacillus Rhamnosus in NLUTD

StatusNot yet recruiting
PhaseEarly Phase 1
SponsorMedstar Health Research Institute
Enrollment48
Study TypeINTERVENTIONAL
ConditionsSpinal Cord Injury; Neurogenic Bladder (NB); Neurogenic Lower Urinary Tract Dysfunction; Multiple Sclerosis; Spina Bifida
Interventions;

The main objective of the proposed research study is to determine in men and women with spinal cord injury/disease and neurogenic bladder whether the dose of coupled gentamicin & Lactobacillus rhamnosus GG affects the recolonization of the bladder, and whether the rate of success differs by sex. Secondary objectives include determining whether that recolonization lasts 7, 14, or 28 days; and s…

NCT07691424 — Impact of Migration History and Social Conditions on the Immuno-virological Control of HIV in Migrants in France

StatusNot yet recruiting
PhaseN/A
SponsorUniversity Hospital, Clermont-Ferrand
Enrollment150
Study TypeOBSERVATIONAL
ConditionsHIV - 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…

NCT07691216 — Retrospective Observational Multicenter Study on the Burden of Hospitalized Patients With Respiratory Tract Infection

StatusNot yet recruiting
PhaseN/A
SponsorLOGEX
Enrollment70000
Study TypeOBSERVATIONAL
ConditionsRespiratory Tract Infections (RTI)
Interventions

This multicenter retrospective real-world data study will evaluate the burden of respiratory tract infection (RTI)-related hospitalizations in up to 10 Dutch hospitals between 2018 and 2026.

The study aims to quantify:

  • Hospitalization rates
  • Healthcare resource utilization (LOS, ICU admissions, readmissions)
  • Clinical outcomes (including mortality)
  • Direct healthcare costs
  • Pathogen-spe…

NCT07578467 — Combining Neo-adjuvant ATR-inhibition With Nodal SBRT for Early-stage Resectable HPV+ OPSCCs

StatusNot yet recruiting
PhasePhase 1 / Phase 2
SponsorAbramson Cancer Center at Penn Medicine
Enrollment35
Study TypeINTERVENTIONAL
ConditionsHPV 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…

NCT07690319 — A Study of Early Secukinumab Treatment in Moderate to Severe Hidradenitis Suppurativa Patients

StatusNot yet recruiting
PhaseN/A
SponsorNovartis Pharmaceuticals
Enrollment186
Study TypeOBSERVATIONAL
ConditionsHidradenitis Suppurativa

The aim of this study is to evaluate the effectiveness of early treatment with secukinumab in patients with moderate-to-severe hidradenitis suppurativa (HS) and assess its impact on disease progression using data from multiple European data sources. All data will be sourced from existing non-interventional study primary data collection, registries, and hospital cohorts that captured information…

NCT06602557 — " Study of the Benefit of Nebulized Amikacin in the Treatment of Gram-negative Bacillus Pneumonia Acquired During Mechanical Ventilation in Patients Receiving Extracorporeal Membrane Veno-arterial Oxygenation “

StatusNot yet recruiting
PhasePhase 2
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment26
Study TypeINTERVENTIONAL
ConditionsPneumonia, Bacterial; Extracorporeal Membrane Oxygenation
Interventions;

Pneumonia are the most frequent infectious complication in patients on Extracorporeal Membrane Oxygenation Veno-arterial (ECMO-VA), with a treatment failure rate of around 40%, even though antibiotic therapy is tailored to the germs identified. One hypothesis to explain this particularly high failure rate is the reduced pulmonary blood flow associated with ECMO offloading of the heart. Although…

Enrolling by Invitation

NCT05350774 — Immunotherapy for Neurological Post-Acute Sequelae of SARS-CoV-2

StatusEnrolling by invitation
PhasePhase 2
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment45
Study TypeINTERVENTIONAL
ConditionsSystemic Inflammation; Neuroinflammation; Microvascular Thrombosis
Interventions;

Background:

COVID-19 can cause problems in different parts of the body. For most people, it causes fevers or trouble breathing. Some people might not recover all the way. Researchers want to see if a treatment can help with people who have recovered from COVID-19 but still have symptoms (“Long COVID”).

Objective:

To learn if human immunoglobulin (IVIG) will help with neurological symptoms of…

NCT07149428 — Longitudinal Deep Phenotyping of Central Mechanisms in Dysosmia: A Pilot Study Using Electrobulbogram (EBG), Functional MRI (fMRI), and Diffusion-Weighted Imaging (DWI)

StatusEnrolling by invitation
PhaseN/A
SponsorNational Institute on Deafness and Other Communication Disorders (NIDCD)
Enrollment80
Study TypeOBSERVATIONAL
ConditionsRespiratory Tract Infection; Smell Disorder; Influenza; Rhinosinusitis; COVID-19

Background:

Loss of the sense of smell can seriously affect a person’s quality of life. The ability to smell can be damaged by many factors, including illnesses, injuries, and exposure to toxic chemicals. The effects can vary, including complete loss of smell, partial loss, and parosomia, which is when things smell differently than they should.

Objective:

To study how brain function changes …

Completed Trials

NCT00004850 — Epidemiology, Infectivity and Natural History of Hepatitis C Virus Infection

StatusCompleted
PhaseN/A
SponsorNational Institutes of Health Clinical Center (CC)
Enrollment805
Study TypeOBSERVATIONAL
ConditionsHepatitis C; Hepatitis B

This study will evaluate hepatitis C virus (HCV) infection in blood donors who test positive for antibodies to this virus. Most HCV-infected people do not become ill and are not aware that they have hepatitis or have had it in the past. Some infected people recover completely, whereas others remain chronically infected. The study will try to define infectivity of anti-HCV positive individuals, …

NCT00001393 — Genetic Markers for Focal Segmental Glomerulosclerosis

StatusCompleted
PhaseN/A
SponsorNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Enrollment616
Study TypeOBSERVATIONAL
ConditionsFocal 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…

NCT00023036 — Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts

StatusCompleted
PhaseN/A
SponsorNational Institute on Deafness and Other Communication Disorders (NIDCD)
Enrollment324
Study TypeOBSERVATIONAL
ConditionsSensorineural Hearing Loss; Cytomegalovirus Infection

This study will try to identify and understand the genetic factors that lead to an inner ear malformation called “enlarged vestibular aqueducts”, that can be associated with hearing loss.

Patients with sensorineural hearing loss with or without inner ear malformations and their parents and siblings may be eligible for this study. Participants and their immediate family members, may undergo som…

NCT01264055 — Cross-sectional Characterization of Idiopathic Bronchiectasis

StatusCompleted
PhaseN/A
SponsorNational Heart, Lung, and Blood Institute (NHLBI)
Enrollment275
Study TypeOBSERVATIONAL
ConditionsInfection; Bronchial Diseases; Respiratory Tract Diseases

Background:

- Bronchiectasis is a type of lung condition in which the lungs airways are abnormally stretched and widened. This stretching and widening makes it difficult for mucus and other substances to move out of the lungs, encouraging the growth of bacteria and leading to breathing problems or infection. Bronchiectasis can be caused by genetic disorders or diseases such as tuberculosis or…

NCT01581554 — Withdrawal of Therapy After Long-Term Antiviral Treatment for Chronic Hepatitis B

StatusCompleted
PhaseN/A
SponsorNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Enrollment15
Study TypeOBSERVATIONAL
ConditionsChronic Hepatitis B e Antigen Positive; Chronic Hepatitis B e Antigen Negative

Background:

- Chronic infection with the hepatitis B virus may lead to cirrhosis, liver disease, and cancer of the liver. There is no cure for the infection, but several drugs have been approved to treat it. These drugs can keep the virus levels low. They seem to be safe for short-term use. But the drugs have not yet been approved for long-term use because some of them can have serious side e…

NCT02694783 — Adoptive Cellular Immunotherapy for Progressive Multifocal Leukoencephalopathy With Ex Vivo Generated Polyomavirus-Specific T-Cells

StatusCompleted
PhaseEarly Phase 1
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment60
Study TypeINTERVENTIONAL
ConditionsProgressive Multifocal Leukoencephalopathy
Interventions

Background:

Progressive Multifocal Leukoencephalopathy (PML) is a brain infection in people with a weakened immune system. Researchers think polyoma virus specific T cells (PyVST) therapy can treat PML. The PyVST cells are made from blood cells of a healthy relative. They are grown in a lab to expand the virus-killing cells, then given to the person with PML.

Objective:

To test whether PyVST…

NCT03534245 — Investigating Vector-Borne Determinants of Aedes Transmitted Arboviral Infections in Cambodia: An Observational Longitudinal Cohort Study in Children

StatusCompleted
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment775
Study TypeOBSERVATIONAL
ConditionsDengue Fever

Background:

Some mosquitos carry viruses that can cause disease. Some examples are dengue and Zika. The mosquitos spread disease by biting people and infecting them with the virus. Children, elderly people, and people who are already sick are especially likely to get infected. Researchers want to learn more to help make new medicines to treat these viral infections.

Objective:

To learn more …

NCT03603808 — VGX-3100 and Electroporation in Treating Patients With HIV-Positive High-Grade Anal Lesions

StatusCompleted
PhasePhase 2
SponsorAIDS Malignancy Consortium
Enrollment44
Study TypeINTERVENTIONAL
ConditionsAnal 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…

NCT04315948 — Trial of Treatments for COVID-19 in Hospitalized Adults

StatusCompleted
PhasePhase 3
SponsorInstitut National de la Santé Et de la Recherche Médicale, France
Enrollment1552
Study TypeINTERVENTIONAL
ConditionsCorona Virus Infection
Interventions; ;

DisCoVeRy is a randomized controlled trial among adults (≥18-year-old) hospitalized for COVID-19. This study is an adaptive, randomized, open or blinded, depending on the drug to be evaluated, clinical trial to evaluate the safety and efficacy of possible therapeutic agents in hospitalized adult patients diagnosed with COVID-19. The study is a multi-centre/country trial that will be conducted i…

NCT05069974 — Alternative Antibiotics for Syphilis

StatusCompleted
PhasePhase 3
SponsorFundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia
Enrollment224
Study TypeINTERVENTIONAL
ConditionsEarly 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…

StatusCompleted
PhaseN/A
SponsorRutgers University
Enrollment36
Study TypeINTERVENTIONAL
ConditionsHIV 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.

NCT05630820 — Study of Bepirovirsen in Nucleos(t)Ide Analogue-treated Participants With Chronic Hepatitis B (B-Well 2)

StatusCompleted
PhasePhase 3
SponsorGlaxoSmithKline
Enrollment857
Study TypeINTERVENTIONAL
ConditionsChronic Hepatitis B; Hepatitis B, Chronic
Interventions;

This study is intended to confirm the efficacy, safety, pharmacokinetic (PK) profile, and the durability of hepatitis B virus surface antigen (HBsAg) suppression observed with bepirovirsen for 24 weeks (with loading doses) as compared to the placebo arm. This study will have 4 stages: a) Double-blind treatment (bepirovirsen or placebo) for 24 weeks. b) Nucleos(t)ide analogue (NA) treatment for …

NCT07690943 — Evaluation of the Safety and Efficacy of Autologous COVID-19 Antigen Specific T Cell in Prolonged SARS-CoV-2 Patients

StatusCompleted
PhaseN/A
SponsorLucasBio
Enrollment13
Study TypeINTERVENTIONAL
ConditionsCOVID-19; COVID-19 (SARS-CoV-2 Infection)
Interventions

The goal of this clinical study is to evaluate the safety and efficacy of autologous COVID-19 antigen specific T cell (LB-DTK-COV19) treatment in prolonged SARS-CoV-2 infected patients. The main questions it aims to answer are:

  • What adverse events occur after the infusion of LB-DTK-COV19?
  • Is there a clinically significant improvement in clinical symptoms within 4 weeks after the infusion? …

NCT07689266 — Soluble Immune Checkpoints in Intra-Abdominal Infections

StatusCompleted
PhaseN/A
SponsorIstanbul Training and Research Hospital
Enrollment75
Study TypeOBSERVATIONAL
ConditionsIntra Abdominal Infections
Interventions

Intraabdominal infections is a life-threatening syndrome with a high incidence and a significant economic burden. The early-stage cytokine storm and the late-stage immunosuppression contribute to the mortality of sepsis. Immune checkpoints expressed on lymphocytes and antigen-presenting cells (APCs) play a crucial role in the pathogenesis of sepsis by regulating immune dysfunction. Specific the…

NCT06404060 — RECOVER-ENERGIZE Platform Protocol_Appendix A (Exercise Intolerance)

StatusCompleted
PhaseN/A
SponsorDuke University
Enrollment360
Study TypeINTERVENTIONAL
ConditionsLong COVID; Long Covid19; Long Covid-19
Interventions;

This is a platform protocol designed to be flexible so that it is suitable for a range of interventions and settings within diverse health care systems and community settings with incorporation into clinical COVID-19 management programs and treatment plans if results achieve key study outcomes.

This protocol is a prospective, multi-center, multi-arm, randomized, controlled platform trial evalu…

NCT06404112 — RECOVER-SLEEP: Platform Protocol, Appendix_B (CPSD)

StatusCompleted
PhasePhase 2
SponsorDuke University
Enrollment469
Study TypeINTERVENTIONAL
ConditionsLong COVID; Long COVID-19; Sleep Disturbance
Interventions; ;

The platform protocol is designed to be flexible so that it is suitable for a range of study settings and intervention types. Therefore, the platform protocol provides a general protocol structure that can be shared by multiple interventions and allows comparative analysis across the interventions. For example, objectives, measures, and endpoints are generalized in the platform protocol, but in…