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AzTrials

Research institution

University of Texas Southwestern Medical Center Clinical Trials

Studies where University of Texas Southwestern Medical Center is the lead sponsor: what is enrolling now, by phase, condition and country.

1,010 registered studies

In numbers

Open to volunteers
198
Active
237
With results posted
311
All registered
1,010

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

Open to volunteers

All 198
  • Surfactant, Respiratory Distress Syndrome (Neonatal)

    Comparing Surfactant Administration Through Supraglottic Airway and Thin Catheter for Preterm Infants

    • Recruiting
    • Age: 0 to 72 hours
    • Surgery or procedure

    What is this study about? This study is comparing two ways of giving surfactant, a medicine that helps premature infants breathe better.

    Trial name
    SALTI (NCT07030270)
    Testing
    Surfactant Administration through Laryngeal or Supraglottic Airway, Surfactant Administration through Thin Catheter
    Where
    United States
    Volunteers
    40 people
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? SALTI
  • Premature Infants, Bronchopulmonary Dysplasia

    Optimization of Saturation Targets And Resuscitation Trial (OptiSTART)

    • Recruiting
    • Age: 0 to 10 minutes

    This study is designed to answer one of the fundamental gaps in knowledge in the resuscitation of preterm infants at birth: What is the optimal target oxygen saturation (SpO2) range that increases survival without long-term…

    Conditions
    Premature Infants, Bronchopulmonary Dysplasia, Intraventricular Hemorrhage, Neurodevelopmental Outcomes
    Trial name
    OptiSTART (NCT05849077)
    Testing
    Sat75, Sat50
    Where
    United States
    Volunteers
    700 people
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? OptiSTART
  • Heart Failure, Acute Decompensated Heart Failure

    Early Discharge With Subcutaneous Furosemide Versus Standard Care in Acute Heart Failure

    • Not yet recruiting
    • Age: 18 to 100 years
    • Phase 3
    • Injection or infusion

    This will be a prospective, cluster-randomized, crossover, non-inferiority trial of 250 participants within 48 hours of an inpatient admission for heart failure or emergency department presentation for heart failure with plans…

    Trial name
    NCT07018297
    Testing
    Early Discharge with Lasix® ONYU (furosemide injection, for subcutaneous use) using SQIN-Infusor
    Where
    2 sites in United States
    Volunteers
    250 people
    Sponsor
    University of Texas Southwestern Medical Center
  • Heart Failure, Diabetes

    Using Ultromics EchoGo HFpEF Algorithm to Identify and Treat High Heart Failure Risk in Patients With Type 2 Diabetes

    • Recruiting
    • Age: All ages
    • Lifestyle or therapy programme

    A pragmatic electronic health record (EHR) based randomized controlled trial to evaluate the utility of providing Ultromics EchoGo analysis results and recommendations for HF risk prevention therapies using an EHR embedded…

    Trial name
    NCT06593314
    Testing
    Message with EchoGo, Standard Message
    Where
    United States
    Volunteers
    800 people
    Sponsor
    University of Texas Southwestern Medical Center
  • Chronic Kidney Disease Mineral and Bone Disorder, Cognitive Function

    REducing Systemic Inflammation With LOw-dose Colchicine to ImproVE Cardiovascular Calcification in Chronic Kidney Disease: A Pilot Randomized Open-Label Trial

    • Not yet recruiting
    • Age: 30 to 69 years
    • Phase 2

    This pilot randomized, open-label, outcome blinded clinical trial is to evaluate the preliminary effects of low-dose Colchicine (LoDoCo) on coronary artery calcification (CAC) progression in adults with chronic kidney disease…

    Conditions
    Chronic Kidney Disease Mineral and Bone Disorder, Cognitive Function, Vascular Calcification, Coronary Artery Calcification
    Trial name
    RESOLVE-CKD (NCT07654231)
    Testing
    Low-dose Colchicine at 0.5mg daily, Usual Care
    Where
    United States
    Volunteers
    60 people
    Sponsor
    University of Texas Southwestern Medical Center
  • Valvular Heart Disease Patients, Aortic Stenosis

    Importance of Point-of-Care Ultrasound for Early Detection of Valvular and Cardiac Diseases (IMPROVE)

    • Not yet recruiting
    • Age: 65 to 85 years
    • Medical device

    Heart valve disease and weakened heart muscle (left ventricular systolic dysfunction) are common in older adults and often go undetected until serious complications such as heart failure develop.

    Conditions
    Valvular Heart Disease Patients, Aortic Stenosis, Mitral Regurgitation, Left Ventricular Diastolic Dysfunction
    Trial name
    IMPROVE (NCT07756398)
    Testing
    Kosmos Torso-One AI-guided Point-of-Care Ultrasound (EchoNous, Inc.)
    Where
    2 sites in United States
    Volunteers
    1,088 people
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? IMPROVE
  • Autism Spectrum Disorder

    Cerebellar Transcranial Direct Current Stimulation (tDCS) in Children With Autism Spectrum Disorder: Raynor Cerebellum Project

    • Recruiting
    • Age: 5 to 21 years
    • Medical device

    The purpose of this research study is to investigate the effects of transcranial direct current stimulation (tDCS) on some of the challenges faced by children with Autism Spectrum Disorder (ASD).

    Trial name
    NCT05691283
    Testing
    trans cranial direct current stimulation (tDCS)
    Where
    United States
    Volunteers
    60 people
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? NCT05691283
  • Anorexia Nervosa

    Cerebellar tDCS Stimulation in Children and Adult Women With Anorexia Nervosa Disorder

    • Recruiting
    • Age: 15 to 30 years
    • Medical device

    Hypothesis: Will the use of tDCS brain modulation in the cerebellum assist in restricted behaviors, social cognition and cognitive flexibility in women with anorexia nervosa in addition to other therapies? Primary Outcomes: 1.

    Trial name
    NCT06286930
    Testing
    anodal trans cranial direct current stimulation (tDCS), cathodal trans cranial direct current stimulation (tDCS)
    Where
    United States
    Volunteers
    15 people
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? NCT06286930
  • Edema, Hypervolemia

    Diuretic Tuner Clinical Decision Support

    • Recruiting
    • Age: 18 years and older
    • Medical device

    This purpose of this study is to determine the effectiveness of a mobile phone application in helping to control body swelling in patients with kidney problems.

    Conditions
    Edema, Hypervolemia, Chronic Kidney Diseases, Nephrotic Syndrome
    Trial name
    NCT04759274
    Testing
    Diuretic Tuner
    Where
    United States
    Volunteers
    30 people
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? NCT04759274
  • Metastatic Renal Cell Carcinoma ( mRCC), OligoProgressive Metastatic Disease

    Radiotherapy in Combination With Checkpoint Inhibition for Patients With Metastatic Kidney Cancer

    • Recruiting
    • Age: 18 years and older
    • Phase 2

    To evaluate the impact of combining innate immune system activation (with IMSA101) with antigen release (through SAbR/PULSAR) on limited progressing lesions during ongoing adaptive immune system activation (with maintenance Nivo).

    Trial name
    SPARK (NCT06601296)
    Testing
    IMSA101
    Where
    United States
    Volunteers
    15 people
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? SPARK

Completed, with results posted

All 249
  • Burn Injury

    Exercise in Burn Survivors: Cooling Modalities

    • Completed
    • Age: 18 to 65 years
    • Results posted

    This project will identify the efficacy of cooling modalities aimed to attenuate excessive elevations in skin and internal body temperatures during physical activity in well-healed burn survivors.

    Trial name
    NCT04512976
    Testing
    Control (no cooling modalities), Water Spray Only, Fan Only
    Where
    United States
    Volunteers
    70 people, healthy volunteers welcome
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? NCT04512976
  • Methamphetamine Use Disorder

    Accelerated Development of Additive Pharmacotherapy Treatment (ADAPT-2) for Methamphetamine Use Disorder

    • Completed
    • Age: 18 to 65 years
    • Phase 3
    • Results posted

    This is a double-blind, placebo-controlled, randomized clinical trial evaluating the efficacy of extended-release naltrexone plus bupropion as a combination pharmacotherapy for methamphetamine use disorder.

    Trial name
    ADAPT-2 (NCT03078075)
    Testing
    Naltrexone: Vivitrol®, Bupropion: Wellbutrin XL®
    Where
    8 sites in United States
    Volunteers
    403 people
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? ADAPT-2
  • Suicide, Attempted, Suicide and Depression

    Ketamine Versus Midazolam for Recurrence of Suicidality in Adolescents

    • Completed
    • Age: 13 to 18 years
    • Phase 3
    • Results posted

    This project aims to examine the signal of efficacy of ketamine, a rapidly acting medication shown to decrease suicidality in adults in as short as hours or days, as opposed to weeks.

    Conditions
    Suicide, Attempted, Suicide and Depression, Suicide Threat
    Trial name
    TASK (NCT04592809)
    Testing
    Ketamine Hydrochloride, Midazolam Hydrochloride
    Where
    United States
    Volunteers
    50 people
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? TASK
  • Major Depressive Disorder, Healthy Controls

    Elucidating the Neurocircuitry of Irritability With High-Field Neuroimaging to Identify Novel Therapeutic Targets

    • Completed
    • Age: 18 to 65 years
    • Phase 2
    • Injection or infusion
    • Results posted

    The study is investigating dysfunctions in neurocircuitry in regards to irritability with healthy controls (HC) and individuals with Major Depressive Disorder (MDD) by performing MRIs.

    Trial name
    UNIKET (NCT05046184)
    Testing
    Ketamine Hydrochloride, Midazolam injection
    Where
    United States
    Volunteers
    104 people, healthy volunteers welcome
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? UNIKET
  • Hyperoxaluria

    A Novel Approach for Reducing Hyperoxaluria and Kidney Stone Risk.

    • Completed
    • Age: 18 to 99 years
    • Phase 4
    • Results posted

    This pilot study is proposing a novel approach to directly target intestinal oxalate absorption with the drug Tenapanor, which was recently FDA-approved for treating hyperphosphatemia in patients with chronic kidney disease.

    Trial name
    NCT06481150
    Testing
    Tenapanor
    Where
    United States
    Volunteers
    18 people, healthy volunteers welcome
    Sponsor
    University of Texas Southwestern Medical Center

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