Records are supplied by study sponsors and investigators. A registry listing is not an endorsement or a guarantee of safety, availability or eligibility.
WCR feed checked: Nov 11, 2026.
RecruitingNCT07645287
HIV-1-infection
Phase 218 years - Not specifiedPhoenix, Arizona, United States +53 The study will have two parts: Part A and Part B. In Part A, the goal of the study is to compare the effectiveness of switching to the study drugs GS-3242 plus Lenacapavir (LEN) versus continuing Biktarvy (bictegravir/emtricitabine/tenofovir alafenam…
RecruitingNCT07927933
Cleft Palate · Cleft Palate +/- Lip · Orofacial Cleft
Not applicable0 months - 12 monthsPhoenix, Arizona, United States This study aims to assess the impact of using a cleft-adapted bottle with a unidirectional valve compared with a non-cleft-adapted bottle on oral volume intake and milk transfer rate.
RecruitingNCT07058077
Heterozygous Familial Hypercholesterolemia (HeFH)
Phase 2 / Phase 36 years - 17 yearsWilmington, Delaware, United States +43 This study is designed to learn if enlicitide decanoate is safe and effective to treat children and adolescents with heterozygous familial hypercholesterolemia (HeFH) and high amounts of low-density lipoprotein cholesterol (LDL-C) in the blood. The g…
RecruitingNCT03407469
Cancer-related Venous Thromboembolism
Observational18 years - Not specifiedHouston, Texas, United States +3 The goal of this research study is to learn about the quality of life, experiences with treatment, and healthcare costs of patients who are receiving long-term treatment for venous thromboembolism (VTE) that is related to cancer. This is an investiga…
RecruitingNCT07592169
SCHIZOPHRENIA 1 (Disorder) · Schizoaffecitve Disorder
Phase 218 years - 55 yearsLa Jolla, California, United States This study is a confirmatory, double-blind, placebo-controlled randomized clinical trial (RCT) testing whether gamma EEG neurofeedback (EEG-NFB) improves working memory in adults with schizophrenia or schizoaffective disorder. Participants are random…
RecruitingNCT00060541
Neurologic Disorders
Observational4 years - 99 yearsBethesda, Maryland, United States Objective: This protocol is designed to allow the Surgical Neurology Branch to evaluate and treat the neurosurgical disorders of protocol participants. The participants will receive standard-of-clinical-care evaluation and treatment. The clinical dat…
SuspendedNCT06577454
Opioid Use Disorder · Healthy Volunteers
Not applicable18 years - 60 yearsBaltimore, Maryland, United States Background: The purpose of this study is to understand how a type of brain stimulation, transcranial magnetic stimulation (TMS), may help those who use opioids such as heroin or methadone. TMS uses brief magnetic pulses to affect brain activity, and …
CompletedNCT07041177
Open Wound
Not applicable18 years - Not specifiedHammond, Louisiana, United States This is a prospective case series evaluating the efficacy and safety of NeoThelium FT Amnion Skin Graft in the Mangement of Open Wounds
Active, not recruitingNCT04973163
Solid Tumors, KRAS Mutation
Phase 118 years - Not specifiedNew York, New York, United States +8 This study is open to adults with different types of advanced or metastatic cancer (including lung cancer, colorectal cancer, pancreatic cancer, and bile duct cancer). This study is for people for whom previous treatment was not successful or no trea…
RecruitingNCT06507930
Breast Cancer · Metastatic Breast Cancer · Advanced Breast Cancer · Unresectable Breast Carcinoma
Not applicable18 years - Not specifiedBoston, Massachusetts, United States The aim of this research study is to better understand the in-home hospice experience for participants, caregivers, hospice nurses, and oncology providers by conducting telehealth check-ins between participants and caregivers and oncology care teams.
CompletedNCT06925919
Rift Valley Fever
Phase 118 years - 64 yearsCypress, California, United States Phase 1 randomized, double-blind, placebo-controlled trial to evaluate safety, tolerability, pharmacokinetics (PK) and immunogenicity of IDB-011 following intramuscular (IM )administration of single ascending doses to healthy adult participants.
RecruitingNCT07144800
Obesity · Child Obesity · Weight Loss
Not applicable18 years - Not specifiedNew York, New York, United States The purpose of this study is to determine the most effective family-centered intervention (FCI) for weight loss and obesity prevention in Hispanic families. FCI is a type of program that involves family (such as parents and caregivers) supporting the…
Retrieved from ClinicalTrials.gov: Nov 11, 2026. Overall study status may differ from a particular location’s status.
