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 Fever from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 22
- Active, not recruiting: 2
- Completed: 11
- Other: 15
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00557726 — Diagnosis and Management of Inflammatory and Infectious Diseases
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 400 |
| Study Type | OBSERVATIONAL |
| Conditions | Infection; Inflammation |
This protocol is being established to cover the evaluation of patients with inflammatory and/or infectious diseases which are not covered under previously existing protocols. The purpose of such a protocol is that frequently patients are referred to us with either diagnosed or undiagnosed illnesses which would be of interest to our teaching program or which would serve as a source of patients t…
NCT00001373 — Familial Mediterranean Fever and Related Disorders: Genetics and Disease Characteristics
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Human Genome Research Institute (NHGRI) |
| Enrollment | 5000 |
| Study Type | OBSERVATIONAL |
| Conditions | Familial Mediterranean Fever (FMF); Autoinflammation; Periodic Fever; Fever; Genetic Diseases |
This study is designed to explore the genetics and pathophysiology of diseases presenting with intermittent fever, including familial Mediterranean fever, TRAPS, hyper-IgD syndrome, and related diseases.
The following individuals may be eligible for this natural history study: 1) patients with known or suspected familial Mediterranean fever, TRAPS, hyper-IgD syndrome or related disorders; 2) r…
NCT01168271 — Host and Parasite Factors That Influence Susceptibility to Malaria Infection and Disease During Pregnancy and Early Childhood in Ouelessebougou and Bamako, Mali
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 15000 |
| Study Type | OBSERVATIONAL |
| Conditions | Malaria |
Malaria caused by Plasmodium falciparum continues to be a global problem with devastating consequences. A greater understanding of the immunologic and parasitologic factors associated with infection and disease is badly needed; and will accelerate the development of highly protective vaccines for both mothers and children. Pregnancy malaria is associated with low birth weight, maternal anemia, …
NCT03510442 — Natural History, Genetics, and Pathophysiology of Systemic Juvenile Idiopathic Arthritis, Adult-Onset Still’s Disease, and Related Conditions
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Still’s Disease, Adult-Onset; Systemic Inflammation; Arthritis; Autoinflammatory Syndrome |
Background:
Inflammatory conditions can cause symptoms like fevers, arthritis, and rash. Systemic juvenile idiopathic arthritis (sJIA) is one of these conditions. So is adult-onset Still s disease (AOSD). Their causes are unknown. Researchers want to learn more about these conditions. This includes genetic changes and environmental factors.
Objective:
To study sJIA and AOSD in children and a…
NCT04034264 — Febrile Disease Landscape in Cambodia Via Metagenomic Pathogen Sequencing
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 6500 |
| Study Type | OBSERVATIONAL |
| Conditions | Vector-Borne Diseases; Emerging Pathogens |
Background:
Vector-borne diseases are caused by the bite of an infected mosquito, fly, flea, tick, or other blood-feeder. These diseases cause almost 1 million deaths per year. And they are on the rise, particularly in Southeast Asia in particular. Researchers think that these diseases make up about 10 percent of fevers in Cambodia. But many of these illnesses are never diagnosed. Studying the…
NCT04088396 — A Study of Baricitinib (LY3009104) in Participants From 1 Year to Less Than 18 Years Old With Systemic Juvenile Idiopathic Arthritis (sJIA)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 58 |
| Study Type | INTERVENTIONAL |
| Conditions | Systemic Juvenile Idiopathic Arthritis |
| Interventions | ; |
The reason for this study is to see if the study drug baricitinib is safe and effective in participants from 1 year to less than 18 years old with systemic juvenile idiopathic arthritis (sJIA). Participants are assigned to 1 of 2 cohorts. In cohort 1, participants will receive baricitinib or tocilizumab reference. In cohort 2, participants will receive baricitinib.
NCT04847063 — Individual Response to Hyperthermic Intraperitoneal Chemotherapy (HIPEC) Treatment of Peritoneal Carcinomatosis From Peritoneal Mesothelioma or Atypical Mesothelial Proliferation or From Ovarian, Colorectal, or Appendiceal Histologies
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Peritoneal Mesothelioma; Peritoneal Carcinomatosis; Ovarian Cancer; Gastrointestinal Cancer; Appendiceal Cancer |
| Interventions | ; ; |
Background:
Cytoreductive surgery (CRS) removes tumors in the abdomen. HIPEC is hyperthermic (heated) chemotherapy that washes the inside of the abdomen. CRS with HIPEC may help people with peritoneal carcinomatosis. These are tumors that have spread to the lining of the abdomen from other cancers. Researchers think they can improve the results of CRS with HIPEC treatment on these tumors by ch…
NCT05631405 — Efficacy of Dengue Infection With Warning Signs Treated With Dexamethasone (DengDex Study)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Chulalongkorn University |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Severe Dengue |
| Interventions | ; |
The goal of this randomized double-blinded placebo-controlled trial is to learn about dexamethasone and the treatment of severe dengue population. The main question it aims to answer are steroid therapy may be effective in dengue.
NCT05419492 — A Clinical Study to Evaluate the Safety and Efficacy of ETX101 in Infants and Children With SCN1A-Positive Dravet Syndrome
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Encoded Therapeutics |
| Enrollment | 47 |
| Study Type | INTERVENTIONAL |
| Conditions | Dravet Syndrome |
| Interventions |
ENDEAVOR is a Phase 1/2, 2-part, multicenter study to evaluate the safety and efficacy of ETX101 in participants with SCN1A-positive Dravet syndrome aged ≥6 to <36 months (Part 1A), aged ≥48 months to <18 years (Part 1B), and aged ≥6 to <48 months (Part 2). Part 1A follows an open-label, dose-escalation design, Part 1B follows an open-label design, and Part 2 is a randomized, double-blind, s…
NCT06665035 — A Study of 2 Doses of Tetravalent Dengue Vaccine (TDV) in Infants and Toddlers
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Takeda |
| Enrollment | 212 |
| Study Type | INTERVENTIONAL |
| Conditions | Dengue Fever |
| Interventions | ; |
Dengue fever is caused by an infection with the dengue virus. Vaccination with Dengue Tetravalent Vaccine (TDV) can help prevent dengue fever. The purpose of this study is to collect information of vaccination with TDV when given to children younger than 2 years. The main aims of this study are to learn how safe the vaccine is and how well it works to activate a young child’s immune system (thi…
NCT06910631 — Optimizing the Care Pathway of Febrile Children Via Capillary C-reactive Protein Assay in Primary Care
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Centre Hospitalier Universitaire de Nīmes |
| Enrollment | 420 |
| Study Type | INTERVENTIONAL |
| Conditions | Fever |
| Interventions |
Fever is the leading reason for outpatient consultations among children aged 2 to 9 years. The main concern in fever is severe bacterial infection, particularly for younger children. History and clinical examination do not always differentiate viral infections from bacterial infection. In 20% of febrile children, no infectious focus is found after examination and additional tests are necessary….
NCT07527247 — Improving Vaccine Protection for Adults
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Singapore General Hospital |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Immune System Responses and Trained Immunity After AS01 Administration; Healthy Adult |
| Interventions | ; ; |
As people grow older, their immune system - the body’s natural defence against diseases - becomes weaker, making them more vulnerable to infections and less responsive to vaccines. This was clearly seen during the COVID-19 pandemic, where older adults were more likely to develop severe illness. Researchers have made an interesting discovery about AS01, an ingredient already used in successful v…
NCT07267598 — Suitability of a 26 °C Indoor Environment for Mitigating Heat Strain in Young Adults
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Ottawa |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Heat Stress; Physiological Stress; Cognitive Change |
| Interventions |
While an indoor upper temperature limit of 26 °C has been shown to protect heat-vulnerable older adults (DOI: 10.1289/EHP11651), this guideline has not been verified in young, habitually active adults. Public health recommendations during hot weather typically emphasize staying in cool environments, avoiding strenuous activity, wearing lightweight clothing, and maintaining adequate hydration. H…
NCT07675746 — A Study to Evaluate the Safety and Pharmacokinetics of RC001 in Children With Dravet Syndrome
| Status | Recruiting |
| Phase | Early Phase 1 |
| Sponsor | Second Affiliated Hospital of Guangzhou Medical University |
| Enrollment | 8 |
| Study Type | INTERVENTIONAL |
| Conditions | Dravet Syndrome (DS) |
| Interventions | ; |
This is an open-label, single-center study to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of intrathecal RC001 in patients with Dravet syndrome aged 2 to 18 years. The study includes a dose-escalation part followed by a fixed dose treatment part, with participant progression based on investigator-assessed safety and efficacy.
NCT07291180 — A Feasibility Study of Mass-Based Response Drug Screening to Guide Personalized Hyperthermic Intraperitoneal Chemotherapy for High-Grade Appendiceal and Colorectal Adenocarcinoma With Peritoneal Metastasis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Yale University |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Appendiceal Cancer; Colorectal Adenocarcinoma; Peritoneal Metastases |
| Interventions |
This study will evaluate the role of mass-based response testing (MRT) to select and deliver personalized hyperthermic intraperitoneal chemotherapy (HIPEC) regimens to patients with peritoneal metastasis (PM) from high-grade appendiceal adenocarcinomas (HGAA) and colorectal cancer (CRC).
NCT07146048 — A Non-Inferiority Trial of Stopping Penicillin in Early Rheumatic Heart Disease: GOAL-Stop
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Children’s Hospital Medical Center, Cincinnati |
| Enrollment | 922 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatic Heart Disease |
| Interventions |
GOAL-Stop is a randomized, controlled, non-inferiority trial designed to evaluate whether discontinuing secondary antibiotic prophylaxis (SAP) is non-inferior to continuing SAP in preventing progression of rheumatic heart disease (RHD) among children and adolescents. The trial will enroll participants aged 5-20 years with previously diagnosed mild RHD who have received at least 2 years of SAP a…
NCT07565090 — A Clinical Study to Investigate the Safety and Immunogenicity of rVSV∆G-SUDV-GP, a Sudan Virus (SUDV) Vaccine for the Prevention of SUDV Disease in Adults in Good General Health
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | International AIDS Vaccine Initiative |
| Enrollment | 112 |
| Study Type | INTERVENTIONAL |
| Conditions | Sudan Virus Disease |
| Interventions | ; |
A Clinical Study to Investigate the Safety and Immunogenicity of rVSV∆G-SUDV-GP, a Sudan Virus (SUDV) Vaccine for the Prevention of SUDV Disease in Adults in Good General Health.
NCT07467707 — An Efficacy, Safety, and Immunogenicity Study of CHIKV VLP Vaccine for the Prevention of Chikungunya Disease in Adolescents and Adults
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Bavarian Nordic |
| Enrollment | 6144 |
| Study Type | INTERVENTIONAL |
| Conditions | Chikungunya Virus |
| Interventions | ; |
Study EBSI-CV-317-007 is a field study to evaluate the efficacy, immunogenicity, and safety of CHIKV VLP vaccine. The study was designed using infectious disease models and advanced analytics to guide region and clinical site prioritization, define the timing of study activities, and optimize the study parameters to local epidemiological conditions for CHIKV disease to overcome the challenges o…
NCT07277387 — Plasma Host-Microbe Proteomics to Predict Complications in High-risk Febrile Neutropenia
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Instituto de Investigación Biomédica de Salamanca |
| Enrollment | 350 |
| Study Type | OBSERVATIONAL |
| Conditions | Febrile Neutropenia |
| Interventions |
Febrile neutropenia (FN) is a common oncologic emergency in patients with hematologic malignancies, associated with high morbidity and mortality. Early identification of patients at higher risk of complications such as sepsis or septic shock is critical to optimize antimicrobial management.
This study aims to characterize the human and microbial plasma proteome using high-resolution mass spect…
NCT07475286 — Combined Systemic and Intraperitoneal Chemotherapy for Synchronous Gastric and/or Gastroesophageal Peritoneal Carcinomatosis
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Mohammad Haroon Asif Choudry |
| Enrollment | 22 |
| Study Type | INTERVENTIONAL |
| Conditions | Synchronous Gastric Peritoneal Carcinomatosis; Gastroesophageal Peritoneal Carcinomatosis |
| Interventions | ; |
This trial will administer laparoscopic hyperthermic intraperitoneal chemotherapy (HIPEC) to patients with peritoneal carcinomatosis from gastric cancer (GPC) who are receiving standard of care systemic chemotherapy.
NCT07664462 — Working in the Heat at Simulated Altitude: Effects of Normobaric Hypoxia on Physiological Strain
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Ottawa |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Body Temperature Changes; Heat Stress; Heat Exposure; Heat Fatigue; Hypoxia, Altitude |
| Interventions | ; |
Extreme heat events are becoming more frequent, intense, and prolonged, increasing the risk of heat-related illness among workers performing physically demanding work in hot environments. Current occupational heat-stress guidelines aim to limit excessive increases in core body temperature and physiological strain through the use of work-rest schedules. However, these guidelines do not provide c…
NCT07683104 — Natural History of Trisomy 8-Associated Autoinflammatory Disease (TRIAD) and Related Disorders
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 750 |
| Study Type | OBSERVATIONAL |
| Conditions | Trisomy 8 Mosaicism; Trisomy 8 Associated Autoinflammatory Disease; Mucosal Ulcerations |
Study Description:
This is a natural history protocol designed to characterize the clinical spectrum of trisomy 8 mosaicism and trisomy 8-associated autoinflammatory disease (TRIAD) and related autoinflammatory disorders and further evaluate approaches to screening, diagnosis, and management. We will enroll affected patients and their unaffected relatives and collect a variety of clinical data…
Active, Not Recruiting
NCT05693545 — GOALIE: Intramuscular vs. Enteral Penicillin Prophylaxis to Prevent Progression of Latent RHD Trial
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Children’s Hospital Medical Center, Cincinnati |
| Enrollment | 1004 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatic Heart Disease |
| Interventions | ; |
The goal of this clinical trial is to determine if twice daily oral penicillin prophylaxis is non-inferior to monthly IM penicillin prophylaxis in preventing latent Rheumatic Heart Disease Progression in children between the ages of 5-17 years. The main objective is to compare the proportion of children aged 5-17 years with latent RHD receiving oral penicillin prophylaxis who progress to worse …
NCT07690956 — Pharmacist-Led Education to Improve Neutropenic Precautions in Cancer Patients
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Jordan University of Science and Technology |
| Enrollment | 300 |
| Study Type | INTERVENTIONAL |
| Conditions | Febrile 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
NCT07621484 — HIPEC Priming Followed by Serplulimab Plus SOX/XELOX in Locally Advanced Gastric Cancer
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Shanghai Changzheng Hospital |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Locally Advanced Gastric Cancer; Gastric Adenocarcinoma; Gastroesophageal Junction Adenocarcinoma |
| Interventions | ; ; |
Patients with locally advanced gastric cancer (LAGC), particularly those with serosal invasion, remain at high risk of peritoneal recurrence despite standard perioperative treatment. Hyperthermic intraperitoneal chemotherapy (HIPEC) may eradicate free intraperitoneal tumor cells and microscopic peritoneal disease while potentially enhancing systemic anti-tumor immune activation.
This is a pros…
NCT07656519 — Consecutive Occupational Heat Exposure With and Without Overnight Cooling
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Ottawa |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Body Temperature Changes; Heat Stress; Heat Exposure; Heat Fatigue; Work Related Stress |
| Interventions | ; |
Extreme heat events are becoming more frequent, intense, and prolonged, increasing the risk of heat-related illness among workers exposed to hot environments. Current occupational heat-stress guidelines are designed to limit excessive increases in core body temperature and physiological strain during work in the heat through the use of work-rest schedules. However, these guidelines are largely …
NCT07690618 — Thermotherapy for Head and Neck Cancer Patients
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | Erasmus Medical Center |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Head and Neck Cancer; Oropharyngeal Carcinoma; Hypopharyngeal Carcinoma; Laryngeal Carcinoma; Head and Neck Squamous Cell Carcinoma |
| Interventions | ; ; |
This phase I, single-center study evaluates the safety, tolerability, and recommended phase II dose (RP2D) of mild hyperthermia (thermotherapy) when added to standard-of-care treatment in patients with locally advanced head and neck squamous cell carcinoma (LAHNSCC). Tumor recurrence remains common despite chemoradiotherapy, highlighting the need for treatment intensification. Thermotherapy, wh…
NCT07688083 — Clinical Validation of Isothermal Nucleic Acid Amplification Bioassays Modules - DRC
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Institute of Tropical Medicine, Belgium |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Ebola Hemorrhagic Fever |
| Interventions |
This study aims to validate the clinical performance of a newly developed isothermal nucleic acid amplification bioassay module for EBOV. A retrospective studies will be conducted using biobanked patient samples such as plasma samples and buccal swabs already collected by the Institut National de Recherches Biomédicales (INRB) in Kinshasa, DRC as part of their surveillance and outbreak activiti…
NCT07681752 — Clinical Validation of Isothermal Nucleic Acid Amplification Bioassays Modules - GUINEA
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Institute of Tropical Medicine, Belgium |
| Enrollment | 150 |
| Study Type | OBSERVATIONAL |
| Conditions | Ebola Hemorrhagic Fever; Lassa Hemorrhagic Fever |
| Interventions |
This study aim to validate the clinical performances of two newly developed isothermal nucleic acid amplification bioassays modules for EBOV and LASV. Two retrospective studies will be conducted using biobanked patient samples such as plasma samples and buccal swabs already collected by the Centre de Recherche en Virologie, Laboratoire des Fièvres Hémorragiques Virales de Guinée (CRV-LFHVG) as …
NCT06599788 — Work Design Interventions for Heat Resilience
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | State University of New York at Buffalo |
| Enrollment | 32 |
| Study Type | INTERVENTIONAL |
| Conditions | Hyperthermia; Fatigue; Heat; Work-Related Condition |
| Interventions | ; ; |
The goal of this project is to compare different ways to schedule a workday to see if older workers should follow a specific work protocol to reduce strain on the heart and muscles.
Participants will come to the lab a total of six times. During four of the visits participants will complete a box carrying task, simulating unloading a delivery truck. This will take place in a hot and humid room …
NCT06144294 — Whole-Body Hyperthermia for Mood and Anxiety Disorders
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Weill Medical College of Cornell University |
| Enrollment | 240 |
| Study Type | INTERVENTIONAL |
| Conditions | Postpartum Depression; Mood Disorders; Anxiety Disorders; Postpartum Anxiety |
| Interventions | ; |
This study aims to examine the scientific mechanisms of whole-body hyperthermia (WBH), a novel, rapidly acting, single session antidepressant and anxiolytic therapy. It also aims to determine its feasibility and acceptability in women with postpartum depression (PPD). The study will enroll four cohorts of participants: healthy postpartum controls; postpartum women with PPD; healthy adult contro…
NCT07046026 — Work Design Interventions for Older Workers During Consecutive Days in the Heat
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | State University of New York at Buffalo |
| Enrollment | 32 |
| Study Type | INTERVENTIONAL |
| Conditions | Hyperthermia; Fatigue; Heat; Work-Related Condition |
| Interventions | ; |
The goal of this project is to compare different ways to schedule a workday to see if older workers should follow a specific work protocol to reduce strain on the heart and muscles across two consecutive days of work.
Participants will come to the lab a total of six times. During four of the visits participants will complete a box carrying task, simulating unloading a delivery truck. This will…
Enrolling by Invitation
NCT07139951 — Hyperthermic Intraperitoneal Chemotherapy With Cisplatin and Paclitaxel for Gastric Cancer at High Risk of Peritoneal Recurrence
| Status | Enrolling by invitation |
| Phase | Phase 2 |
| Sponsor | Mayo Clinic |
| Enrollment | 16 |
| Study Type | INTERVENTIONAL |
| Conditions | Clinical Stage I Gastric Cancer AJCC v8; Clinical Stage I Gastroesophageal Junction Adenocarcinoma AJCC v8; Clinical Stage II Gastric Cancer AJCC v8; Clinical Stage II Gastroesophageal Junction Adenocarcinoma AJCC v8; Clinical Stage III Gastric Cancer AJCC v8 |
| Interventions | ; ; |
This phase II trial tests how well concentrating heated (hyperthermic) chemotherapy in the area that contains the abdominal organs (intraperitoneal [IP]) at the time of surgery works in treating patients with gastric or gastroesophageal junction adenocarcinoma at high risk of the cancer coming back to the abdominal cavity (peritoneal) after a period of improvement (recurrence). Recurrence in …
NCT07499128 — Continuous Temperature Monitoring (CTM) for Cytokine Release Syndrome (CRS), an Immune-Related Adverse Event
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 136 |
| Study Type | INTERVENTIONAL |
| Conditions | Cytokine Release Syndrome; Neoplasms; Lymphoma; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Multiple Myeloma |
| Interventions | ; |
Background:
Drugs or cell therapies to treat cancer can sometimes cause cytokine release syndrome (CRS). That is, the body makes too many cytokines after treatment. Cytokines are proteins that play a role in the immune system. CRS can cause fever, chills, fatigue, low blood pressure, or breathing problems. Researchers want to know if continuously monitoring a person s body temperature can help…
NCT07678619 — Smart Analysis and Decision-Making for Emerging Infectious Diseases
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Peking University |
| Enrollment | 780 |
| Study Type | INTERVENTIONAL |
| Conditions | Emerging Infectious Diseases; COVID-19; Influenza; Mpox (Monkeypox); Dengue Fever |
| Interventions | ; |
Emerging infectious diseases, such as COVID-19, mpox, and dengue fever, are characterized by rapid transmission, wide impact, and high uncertainty, posing ongoing threats to global public health. While China achieved significant success in COVID-19 control, the response also revealed key challenges, including fragmented information, delayed risk perception, experience-dependent assessment, and …
Completed Trials
NCT01972347 — Neoadjuvant Dabrafenib + Trametinib for AJCC Stage IIIB-C BRAF V600 Mutation Positive Melanoma
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Melanoma Institute Australia |
| Enrollment | 35 |
| Study Type | INTERVENTIONAL |
| Conditions | Melanoma |
| Interventions | ; |
This is an open label, single centre, phase II study of neoadjuvant drug treatment with dabrafenib + trametinib in patients with resectable American Joint Committee on Cancer (AJCC) Stage IIIB-C BRAF V600 mutation positive melanoma.
The main aim of this study is to find out if giving of a new combined drug treatment to patients with melanoma that has spread to the lymph nodes BEFORE they have …
NCT03534245 — Investigating Vector-Borne Determinants of Aedes Transmitted Arboviral Infections in Cambodia: An Observational Longitudinal Cohort Study in Children
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 775 |
| Study Type | OBSERVATIONAL |
| Conditions | Dengue 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 …
NCT03783143 — Prevalence and Incidence of Lassa Virus Infection in Southern Mali
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 8524 |
| Study Type | OBSERVATIONAL |
| Conditions | Lassa Virus Infection |
Background:
The disease Lassa fever mostly affects people in Western Africa. It is very similar to other diseases that cause fever, like malaria and yellow fever. People get Lassa fever from mice infected with Lassa virus. It can also be spread from body fluids of people with the disease. Researchers want to learn more about this virus in Mali so they can develop better tools to diagnose and p…
NCT04727242 — CytoreductiveSurgery & HIPEC w/Gemcitabine+Chemotherapy w/Dacarbazine in Uterine Leiomyosarcoma
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Stanford University |
| Enrollment | 17 |
| Study Type | INTERVENTIONAL |
| Conditions | LMS - Leiomyosarcoma; Uterine Leiomyosarcoma |
| Interventions | ; ; |
The purpose of this study is to find out if giving a dose of heated chemotherapy in the abdomen immediately after surgery that is done to remove uterine leiomyosarcoma type of cancer will help lower the risk of the cancer coming back in the future.
NCT04415944 — Trial Evaluating Feasibility and Quality of Life of Second Look Laparoscopy With Hyperthermic Intraperitoneal Chemotherapy
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Wake Forest University Health Sciences |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Ovarian Epithelial Cancer Stage I; Ovarian Epithelial Cancer Stage II; Ovarian Epithelial Cancer Stage III; Stage I Fallopian Tube Cancer; Stage II Fallopian Tube Cancer |
| Interventions | ; ; |
The purpose of this research study is to see if it is feasible to receive heated chemotherapy or heated intraperitoneal chemotherapy (HIPEC) inserted directly into the abdomen at the time of a Second Look Reassessment Surgery and to monitor any effects good or bad that this has on participants’ health.
NCT07660003 — 8-OHdG and Oxidative Stress in Febrile Seizures
| Status | Completed |
| Phase | N/A |
| Sponsor | Kayseri City Hospital |
| Enrollment | 156 |
| Study Type | OBSERVATIONAL |
| Conditions | Febrile Seizures; Oxidative Stress; Oxidative DNA Damage |
| Interventions | ; ; |
This prospective case-control study investigates whether serum 8-hydroxy-2’-deoxyguanosine (8-OHdG), an established biomarker of reactive oxygen species-mediated DNA oxidation, is elevated in children with febrile seizures compared with healthy children, and whether it differs between simple and complex febrile seizure subtypes. Children presenting with a febrile seizure and age-matched healthy…
NCT05157191 — Safety of Pediatric COVID-19 Vaccination
| Status | Completed |
| Phase | N/A |
| Sponsor | Duke University |
| Enrollment | 299 |
| Study Type | OBSERVATIONAL |
| Conditions | Pain; Injection Site Reaction; Adverse Drug Event |
| Interventions |
This is a prospective, observational study. During the study, children and adolescents (ages ≥ 5 to < 16) will be followed post administration of mRNA COVID-19 vaccines.
Injection site (local), systemic reaction, and unsolicited adverse event data will be assessed on vaccination day and during the 7 days following each vaccination using either identical web-based or paper diaries, depending o…
NCT06121934 — Efficacy and Safety of Carica Papaya in Dengue Fever: A Randomised Clinical Trial
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh |
| Enrollment | 250 |
| Study Type | INTERVENTIONAL |
| Conditions | Dengue |
| Interventions | ; |
This will be a placebo-controlled, multicenter-randomized prospective study of CPLE (Carica papaya leaf extract) tabs in dengue patients (WHO-Group A, B). The study will enroll 300 eligible dengue cases into two arms: one arm receiving CPLE 1000mg t.i.d for 5 days and the other group receiving a placebo.
The main question to ask is whether CPLE reduces severe disease progression and increases …
NCT06676020 — Effect of Febrile Convulsion Training on Anxiety and Knowledge
| Status | Completed |
| Phase | N/A |
| Sponsor | Uskudar University |
| Enrollment | 66 |
| Study Type | OBSERVATIONAL |
| Conditions | Febrile Convulsion |
The research will be conducted to determine the effect of the training given to parents/caregivers on their knowledge, attitudes, practices and anxiety towards preventing febrile seizures in children. The research will be carried out as a randomised controlled experimental design in the Pediatric Emergency Department of Zeynep Kamil Women’s and Children’s Diseases Training and Research Hospital…
NCT06811129 — Long-Term Neurologic and Neurocognitive Sequelae Following Pediatric Ebola Virus in Liberia
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 328 |
| Study Type | OBSERVATIONAL |
| Conditions | Ebola; Post-Acute Ebola Syndrome |
Background:
Ebola virus disease (EVD) causes fever, vomiting, and diarrhea, and may cause internal bleeding. It is often fatal. EVD may also damage the brain and nervous system. It can cause headaches, tremors, weakness, and other problems. These issues can continue for years after people recover from EVD infection. Researchers want to understand more about how EVD may have affected the brains…
NCT06855576 — Bioequivalence Study of Paracetamol With Oral Single Dose Administration in Healthy Adult Subjects Under Fasting Conditions
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | HALEON |
| Enrollment | 54 |
| Study Type | INTERVENTIONAL |
| Conditions | Fever; Pain |
| Interventions | ; ; |
This study aims to evaluate the bioequivalence of new formulated orodispersible tablet (ODT) containing 500 milligram (mg) paracetamol in comparison to the European marketed Alvedon (paracetamol) 500 mg film-coated tablets and the Australian marketed Panadol (paracetamol) 500 mg film-coated tablets as reference products.
Other (Suspended)
NCT02483260 — Intravenous Ribavirin Protocol to Treat Individuals With Viral Hemorrhagic Fever
| Status | Suspended |
| Phase | N/A |
| Sponsor | U.S. Army Medical Research and Development Command |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Viral Hemorrhagic Fever |
| Interventions |
Is ribavirin a therapeutic option for patients with a probable or suspected case of viral hemorrhagic fever?
NCT04283513 — Treatment of Hemorrhagic Fever With Ribavirin
| Status | Suspended |
| Phase | Phase 2 |
| Sponsor | U.S. Army Medical Research and Development Command |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Hemorrhagic Fever |
| Interventions |
Multisite protocol to provide IV Ribavirin treatment to patients with probable or suspected case of Hemorrhagic Fever with Renal Syndrome (HFRS)
NCT07419373 — ARN-75039 Lassa Fever Treatment in West Africa
| Status | Suspended |
| Phase | Phase 2 |
| Sponsor | Arisan Therapeutics, Inc. |
| Enrollment | 135 |
| Study Type | INTERVENTIONAL |
| Conditions | Lassa Fever |
| Interventions | ; ; |
This multicenter, randomized, open-label Phase 2 clinical trial evaluates the safety, tolerability, and virologic efficacy of ARN-75039, a novel oral antiviral, for treating Lassa fever in hospitalized adults in West Africa. The study is conducted within the INTEGRATE platform and compares two oral dose regimens of ARN-75039 (100 mg BID and 50 mg BID) with intravenous ribavirin, the locally man…
Other (Withdrawn)
NCT06666335 — A Study to Evaluate Efficacy and Safety of Anakinra in Chinese Patients With Colchicine-resistent FMF
| Status | Withdrawn |
| Phase | Phase 4 |
| Sponsor | Swedish Orphan Biovitrum |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Familial Mediterranean Fever (FMF ) |
| Interventions |
The purpose of this study is to evaluate the efficacy and safety of anakinra in Chinese patients with colchicine-resistand Familial Mediterranian Fever (FMF). The study consists of up to one month screening, to see if a patient is suitable to the study, 6 months of treatment with anakinra and one month safety follow up after last dose of anakinra. In total 3 patients, male and female from 2 yea…