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Research institution

University of Louisville Clinical Trials

Studies where University of Louisville is the lead sponsor: what is enrolling now, by phase, condition and country.

291 registered studies

In numbers

Open to volunteers
41
Active
46
With results posted
51
All registered
291

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 41
  • Eating Disorders

    Be Body Brave: Digital Written Exposure Therapy for Eating Disorders

    • Not yet recruiting
    • Age: 18 to 65 years
    • Lifestyle or therapy programme

    Current eating disorder (ED) treatment options are both inaccessible (80% of people with EDs do not access treatment) and not entirely successful (most people with an ED do not reach full remission).

    Trial name
    BBB (NCT07914712)
    Testing
    Imaginal exposure, Eating disorder journaling
    Volunteers
    900 people
    Sponsor
    University of Louisville
    Can I take part? BBB
  • Financial Toxicity, Cancer

    Implementing Stepped Financial and Legal Navigation to Mitigate Financial Toxicity in Adolescent and Young Adult Cancer Patients Oncology Financial and Legal Navigation (OFLN)

    • Not yet recruiting
    • Age: 18 to 39 years

    The overall objective of this study is to test the effectiveness and implementability of stepped Oncology Financial and Legal Navigation (OFLN) in a noninferiority randomized controlled trial (RCT) using a hybrid type 1…

    Conditions
    Financial Toxicity, Cancer, Adolescent, Young Adult Cancer Survivors
    Trial name
    OFLN (NCT07849699)
    Testing
    Oncology Financial and Legal Navigation (OFLN) Stepped: Low Intensity, Oncology Financial and Legal Navigation (OFLN) Standard, Oncology Financial and Legal Navigation (OFLN) Stepped: High-Intensity
    Where
    United States
    Volunteers
    294 people
    Sponsor
    University of Louisville
    Can I take part? OFLN
  • Spinal Cord Injuries

    Neuromodulation of Spinal Locomotor Circuitry to Elicit Stepping After Pediatric Spinal Cord Injury

    • Enrolling by invitation
    • Age: 4 to 12 years
    • Medical device

    Spinal cord injury (SCI) results in damage to the descending neural pathways and leads to the immediate dysfunction of multiple physiological systems below the level of injury.

    Trial name
    NCT04077346
    Testing
    Biostim-5 transcutaneous spinal stimulator, Transcutaneous Spinal Stimulator + Activity Based Locomotor Training
    Where
    United States
    Volunteers
    8 people
    Sponsor
    University of Louisville
    Can I take part? NCT04077346
  • Spinal Cord Injuries

    Transcutaneous Spinal Stimulation: Safety and Feasibility for Upper Limb Function in Children With Spinal Cord Injury

    • Enrolling by invitation
    • Age: 4 to 18 years
    • Medical device

    Children who suffer a spinal cord injury in the neck region have difficulty using their hands due to paralysis and/or weakness of their arms and hand muscles.

    Trial name
    NCT04032990
    Testing
    Biostim-5 transcutaneous spinal stimulator
    Where
    United States
    Volunteers
    10 people
    Sponsor
    University of Louisville
    Can I take part? NCT04032990
  • Perinatal Spinal Cord Injury

    Understanding Perinatal Spinal Cord Injury

    • Recruiting
    • Age: 3 to 8 years
    • Medical device

    The purpose of this study is to deepen our understanding of children who have a cervical spinal cord injury obtained in utero or at birth and examine the effects of tailored activity-based recovery training (ABRT) in combination…

    Trial name
    NCT06808035
    Testing
    Activity-Based Recovery Training, Transcutaneous Spinal Cord Stimulation
    Where
    United States
    Volunteers
    6 people
    Sponsor
    University of Louisville
    Can I take part? NCT06808035
  • Traumatic Brain Injury (TBI) Patients

    Saline Versus Balanced Crystalloid in Traumatic Brain Injury

    • Recruiting
    • Age: 18 years and older
    • Phase 3

    The goal of this clinical trial is to determine which crystalloid (saline or balanced) should be used in the critical management of Traumatic Brain Injury (TBI) in moderate or severe TBI patients.

    Trial name
    FLUID-TBI (NCT06953674)
    Testing
    Normal Saline (0.9% NaCl), balanced crystalloid
    Where
    United States
    Volunteers
    600 people
    Sponsor
    University of Louisville
    Can I take part? FLUID-TBI
  • Alcohol Use Disorder, Alcohol-associated Liver Disease

    Pomegranate Dietary Supplements in AUD and ALD

    • Not yet recruiting
    • Age: 18 years and older
    • Observational study

    The goal of this project is to determine an individual's ability to generate active gut microbial metabolites called urolithins upon consumption of pomegranate dietary supplements.

    Conditions
    Alcohol Use Disorder, Alcohol-associated Liver Disease, Alcoholic Cirrhosis, Healthy
    Trial name
    NCT07678567
    Testing
    Pomegranate Dietary Ssupplement
    Where
    United States
    Volunteers
    144 people, healthy volunteers welcome
    Sponsor
    University of Louisville
    Can I take part? NCT07678567
  • Brain Metastases

    MeDex: No Perioperative Dexamethasone in Brain Metastases

    • Recruiting
    • Age: 18 years and older

    Perioperative treatment of newly diagnosed cancer patients with brain metastasis without dexamethasone (Dex).

    Trial name
    NCT07044557
    Testing
    Withholding perioperative Dexamethasone
    Where
    United States
    Volunteers
    35 people
    Sponsor
    University of Louisville
    Can I take part? NCT07044557
  • Aneurysmal Subarachnoid Hemorrhage

    Dome-Only Aneurysm Coiling in Severe Aneurysmal Subarachnoid Hemorrhage

    • Recruiting
    • Age: 18 years and older
    • Observational study

    The DOME study is a clinical trial exploring a new treatment approach for patients who suffered a severe brain bleed due to an aneurysm.

    Trial name
    DOME (NCT07250958)
    Where
    United States
    Volunteers
    30 people
    Sponsor
    University of Louisville
    Can I take part? DOME
  • Vision

    Intermediate Visual Space Perception

    • Recruiting
    • Age: 18 to 40 years

    The ability to judge the locations of various objects from oneself during self-motion in the intermediate distance range (~2-25m) is crucial for successful performance of activities of daily living, such as walking and driving.

    Trial name
    NCT05419713
    Testing
    Visual Stimuli for Space Perception
    Where
    United States
    Volunteers
    180 people, healthy volunteers welcome
    Sponsor
    University of Louisville

Completed, with results posted

All 34
  • Urinary Bladder, Neurogenic, Blood Pressure

    Recovery of Bladder and Sexual Function After Human Spinal Cord Injury

    • Completed
    • Age: 18 to 70 years
    • Observational study
    • Results posted

    This study will incorporate critical cross viscero-visceral intersystem interactions to investigate in a controlled laboratory setting the extent, severity, and frequency of occurrence of autonomic dysreflexia with respect to…

    Conditions
    Urinary Bladder, Neurogenic, Blood Pressure, Autonomic Dysreflexia, Bowel Incontinence
    Trial name
    NCT04193709
    Where
    United States
    Volunteers
    57 people
    Sponsor
    University of Louisville
    Can I take part? NCT04193709
  • Air Pollution Toxicity

    Nucleophilic Defense Against PM Toxicity (NEAT Trial)

    • Completed
    • Age: 22 to 65 years
    • Results posted

    Carnosine is a naturally occurring peptide found in high levels in skeletal muscle and the brain and is also available commercially as a dietary supplement.

    Trial name
    NEAT (NCT03314987)
    Testing
    L-carnosine
    Where
    United States
    Volunteers
    299 people, healthy volunteers welcome
    Sponsor
    University of Louisville
    Can I take part? NEAT
  • Overactive Bladder, Urge Incontinence

    Lidocaine Patches Prior to Percutaneous Nerve Evaluation

    • Completed
    • Age: 18 years and older
    • Phase 2
    • Results posted

    The study will be a double-blind randomized control trial comparing 4% lidocaine patch placed over the sacrum 3 minutes prior to a percutaneous nerve evaluation (PNE) procedure to a placebo patch in patients already scheduled to…

    Conditions
    Overactive Bladder, Urge Incontinence, Fecal Incontinence
    Trial name
    NCT05783219
    Testing
    Lidocaine patch
    Where
    2 sites in United States
    Volunteers
    39 people, healthy volunteers welcome
    Sponsor
    University of Louisville
  • Neurogenic Bladder, Spinal Cord Injuries

    Gentamicin Bladder Instillation in Individuals With Spinal Cord Injury Having Chronic Urinary Tract Infections

    • Completed
    • Age: 18 years and older
    • Phase 2
    • Results posted

    Participants will undergo daily gentamicin bladder instillations to determine if its use will reduce the rate of symptomatic urinary tract infections (UTIs) as well as the use of oral and intravenous antibiotics in adults with…

    Trial name
    NCT03931408
    Testing
    Gentamicin Sulfate, No instillation
    Where
    United States
    Volunteers
    6 people
    Sponsor
    University of Louisville
    Can I take part? NCT03931408
  • Spinal Cord Injuries

    Recovery of Bladder and Sexual Function After Spinal Cord Injury

    • Completed
    • Age: 18 years and older
    • Surgery or procedure
    • Results posted

    Bladder and sexual dysfunction consistently ranks as one of the top disorders affecting quality of life after spinal cord injury.

    Trial name
    NCT03036527
    Testing
    Activity-based locomotor training, Activity-based stand training, Activity-based upper arm ergometry
    Where
    United States
    Volunteers
    40 people, healthy volunteers welcome
    Sponsor
    University of Louisville
    Can I take part? NCT03036527

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