A Study to Test Whether Survodutide Improves How the Body Uses Energy and Breaks Down Fat in People With Obesity
Recruiting
This study is open to adults between 18 and 65 years of age who have obesity. People can join the study if they have a body mass index (BMI) between 30 and 45 km/m². The purpose of this study is to find out whether a medicine called survodutide improves how the body uses energy and breaks down fat. This study compares survodutide with another medicine called semaglutide. Survodutide is being developed to treat people with obesity. Semaglutide is already used to treat people with obesity. Parti... Read More
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
06/09/2025
Locations: Translational Research Institute for Metabolism and Diabetes, Orlando, Florida +1 locations
Conditions: Obesity
To Investigate the Efficacy of Treatment With Oral NA-921 (Bionetide) Versus Placebo in Females With Rett Syndrome
Recruiting
Primary Objective • To investigate the efficacy of treatment with oral Bionetide versus placebo in girls and women with Rett syndrome Key Secondary Objective • To investigate the efficacy of treatment with oral Bionetide versus placebo on ability to communicate in girls and women with Rett syndrome
Gender:
FEMALE
Ages:
Between 5 years and 20 years
Trial Updated:
06/09/2025
Locations: Biomed Testing Facility # BIO-01-85012, Phoenix, Arizona +23 locations
Conditions: Rett Syndrome
A Study to Evaluate the Safety of a Delivery Device for Administering LCTOPC1 in Participants With Spinal Cord Injury
Recruiting
The DOSED clinical study evaluates the safety and utility of a novel delivery device to deliver LCTOPC1, a cell therapy, to the spinal cord of patients with a spinal cord injury (SCI). LCTOPC1 is designed to replace or support cells that are absent or dysfunctional due to traumatic injury, with a goal to help improve the quality of life and restore or augment functional activity in persons suffering from a traumatic cervical or thoracic injuries.
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
06/09/2025
Locations: University of California, San Diego, La Jolla, California
Conditions: Spinal Cord Injury Cervical, Spinal Cord Injury Thoracic, Spinal Cord Injury, Acute, Spinal Cord Injury, Spinal Cord Injury, Chronic
Belongingness in Nursing Through Mindfulness - BEING Mindful: A Pilot Study
Recruiting
The long-term goal of this study is to develop a mindfulness-based intervention (MBI) program to reduce stress and burnout while increasing belongingness and connectedness among faculty and staff at the University of New Mexico (UNM) College of Nursing (CON). The central hypothesis is that the MBI intervention will improve psychosocial outcomes (sense of belonging) and physiological outcomes (heart rate variability, HRV) among CON faculty and staff. The specific aims are to: Aim 1: Evaluate th... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
06/09/2025
Locations: University of New Mexico College of Nursing, Albuquerque, New Mexico
Conditions: Mindfulness, Sense of Belonging
HealthySteps + PlayReadVIP
Recruiting
This study aims to investigate the effectiveness and implementation outcomes for the integration of two evidence-based practices and interventions (EBPIs) within pediatric primary care settings: HealthySteps (HS), which provides parenting support, and PlayReadVIP, which promotes relational health through video coaching. Families will be randomized to receive either the integrated HS + PlayReadVIP model or traditional HS, and investigators will examine impacts on parenting, parent-child relations... Read More
Gender:
ALL
Ages:
6 months and below
Trial Updated:
06/09/2025
Locations: NYU Langone Health, New York, New York
Conditions: Families With Infants
The Prevalence of Directional Preference in the Lumbar Stenosis Population
Recruiting
This will be a prospective cohort observational study observing patients with low back pain with leg pain who present for outpatient physical therapy care at Rusk Rehabilitation at NYU Langone Ambulatory Care Lake Success. Patients are eligible if they present with imaging of stenosis in their lumbar spine on MRI or CT Scan and note radicular leg symptoms with associated neurological deficits on the physical examination for at least 12 weeks.
Gender:
ALL
Ages:
48 years and above
Trial Updated:
06/09/2025
Locations: NYU Langone Health, Lake Success, New York
Conditions: Lumbar Stenosis
Characterization and Analysis of Evoked Cortical Responses in Participants With Medication-intractable Epilepsy
Recruiting
The goal of this project is to study how the brain reacts to a small electrical signal. Researchers will be using a novel combination of recording electrodes. The researchers will measure the brain response from these electrodes.
Gender:
ALL
Ages:
Between 22 years and 75 years
Trial Updated:
06/09/2025
Locations: University of Michigan, Ann Arbor, Michigan
Conditions: Intractable Epilepsy
Reactions to Distress (RED) In Louisville, KY Study
Recruiting
The goal of this study is to understand whether race-related stress can impact the way people direct their attention and what interventions may be helpful for attention.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
06/09/2025
Locations: Davidson Hall, Louisville, Kentucky
Conditions: Threat Sensitivity
A Study of Andecaliximab in People With Spinal Cord Injury at Risk for Bone Growth Outside of the Normal Skeleton.
Recruiting
This is an open-label study of andecaliximab in participants at risk of developing bone where bone should not be, such as in muscle, tendons, and other soft tissues following traumatic spinal cord injury. The goal of this study is to assess the safety of andecaliximab, how much drug is in the body over time (pharmacokinetics/PK), and how it affects the body (pharmacodynamics/PD) in participants who have had a recent traumatic spinal cord injury.
Gender:
ALL
Ages:
Between 18 years and 89 years
Trial Updated:
06/09/2025
Locations: Craig Hospital, Denver, Colorado
Conditions: Heterotopic Ossification (HO)
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy of ASC50 Tables in Healthy Participants and Participants With Plaque Psoriasis
Recruiting
This is a phase I, randomized, double-blind, placebo-controlled, single and multiple ascending dose study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, food effect of ASC50 tablets in healthy adult participants and adult participants with mild to moderate plaque psoriasis.
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
06/09/2025
Locations: Ascletis Clinical Site, Miami, Florida
Conditions: Plaque Psoriasis
Multilevel Community-Centered Intervention to Reduce Pregnancy Related and Associated Morbidity and Mortality (PRAMM) Disparities
Recruiting
The goal of the study involving human subjects is to train providers to address patient-provider interactions. The study will survey providers to assess pre-post knowledge, understanding, and behavior changes.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
06/09/2025
Locations: Strong Beginings, Grand Rapids, Michigan
Conditions: Provider Confidence, Provider Behavior
Effects of Hip Bump Manipulation Versus Sham Treatment in Healthy Adults
Recruiting
The purpose of this study is to objectively assess the effects of hip bump manipulation (HBM) on a healthy population aged 18-45 years. We hypothesize that the HBM will improve hip internal rotation passive range of motion, improve the strength of the hip external rotators, decrease compensatory motions in hip flexion during active range of motion, and improve bipodal landing mechanics. Human participants will be analyzed to determine whether the manipulation produces the intended clinical outc... Read More
Gender:
ALL
Ages:
Between 18 years and 45 years
Trial Updated:
06/09/2025
Locations: Dominican University New York, Orangeburg, New York
Conditions: Hip Function, Hip External Rotator Strength, Hip Internal Rotation Range of Motion, Bipodal Landing, EMG Activation