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Research institution

Stanford University Clinical Trials

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

2,161 registered studies

In numbers

Open to volunteers
406
Active
475
With results posted
546
All registered
2,161

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

Open to volunteers

All 406
  • Schizophrenia Disorder, Schizoaffective Disorder

    Incentives and Long-Acting Injectable Adherence After Involuntary Hospitalization

    • Enrolling by invitation
    • Age: 18 to 65 years
    • Injection or infusion
    • Lifestyle or therapy programme

    This study is a randomized controlled trial evaluating the impact of financial incentives on medication adherence among individuals with schizophrenia, schizoaffective disorder, or bipolar disorder and/or co-occurring substance…

    Conditions
    Schizophrenia Disorder, Schizoaffective Disorder, Bipolar Disorder (BD), Substance Use Disorder (SUD)
    Trial name
    NCT07130500
    Testing
    Financial incentives for adherence to long-acting injectable medication, Standard of care with monthly surveys
    Where
    6 sites in United States
    Volunteers
    1,000 people
    Sponsor
    Stanford University
    Can I take part? NCT07130500
  • Glaucoma

    Topical Insulin for Glaucoma

    • Recruiting
    • Age: 18 years and older
    • Phase 1

    The purpose of this Phase 1 trial is to determine the safety over 1-2 months of topic sterile human recombinant insulin on subjects with optic neuropathies (glaucoma, ischecmic optic neuropathy, and optic disc drusen).

    Trial name
    TING1 (NCT05206877)
    Testing
    Insulin, 4 units, Insulin, 20 units, insulin, 4 units twice daily
    Where
    United States
    Volunteers
    52 people
    Sponsor
    Stanford University
    Can I take part? TING1
  • Alcohol Abuse, Alcohol Use Disorder

    A SMART Evaluation of an Adaptive Web-based AUD Treatment for Service Members and Their Partners

    • Recruiting
    • Age: 18 years and older
    • Lifestyle or therapy programme

    The purpose of this study is to evaluate the efficacy of an adaptive web intervention (Partners Connect) on military spouse drinking behaviors (CPs) and service member help-seeking (SMs).

    Conditions
    Alcohol Abuse, Alcohol Use Disorder, Alcohol Drinking, Relations, Interpersonal
    Trial name
    NCT05619185
    Testing
    CRAFT Web-Based Intervention, Phone-Based CRAFT, CRAFT Workbook
    Where
    United States
    Volunteers
    744 people, healthy volunteers welcome
    Sponsor
    Stanford University
    Can I take part? NCT05619185
  • Chronic Pain, Cesarean Section Complications

    Reducing Chronic Pain Following Cesarean Delivery

    • Recruiting
    • Age: 18 years and older
    • Lifestyle or therapy programme

    This pilot study will evaluate the feasibility and acceptability of delivering Empowered Relief (ER), a single-session pain relief skills class, to postpartum women with ongoing pain and/or pain interference following cesarean…

    Conditions
    Chronic Pain, Cesarean Section Complications, Postpartum
    Trial name
    NCT07799883
    Testing
    Empowered Relief
    Where
    United States
    Volunteers
    30 people
    Sponsor
    Stanford University
    Can I take part? NCT07799883
  • Major Depressive Disorder (MDD)

    Sedation and Guided Education for Depression Study

    • Not yet recruiting
    • Age: 18 years and older
    • Injection or infusion
    • Lifestyle or therapy programme

    The goal of this clinical trial is to understand how patient education surrounding a one-time, consciousness-altering medical intervention impacts the antidepressant response to the intervention in adults with major depressive…

    Trial name
    SAGE (NCT06705270)
    Testing
    Response-focused education, Diagnosis-focused education, IV naloxone
    Volunteers
    40 people
    Sponsor
    Stanford University
    Can I take part? SAGE
  • Post-Bariatric Hypoglycemia

    Dietary, Medication, and Endoscopic Interventions for Post-Bariatric Hypoglycemia

    • Not yet recruiting
    • Age: 18 to 70 years
    • Lifestyle or therapy programme

    Post-bariatric hypoglycemia (PBH) is a complication of upper gastrointestinal surgery that causes recurrent episodes of low blood sugar after eating and can substantially impair quality of life.

    Trial name
    NCT07878494
    Testing
    Dietary Intervention, GLP-1 receptor agonist or Dual GIP/GLP-1 receptor agonist, Transoral Outlet Reduction (TORe)
    Where
    United States
    Volunteers
    30 people
    Sponsor
    Stanford University
    Can I take part? NCT07878494
  • ACL Tear

    Quadriceps Strengthening ACL Reconstruction

    • Recruiting
    • Age: 13 to 17 years

    The purpose of this study is to characterize quadriceps function and squat biomechanics during the early strengthening phase in adolescent patients undergoing a standardized combined neuromuscular electrical stimulation (NMES)…

    Trial name
    ACL (NCT07015541)
    Testing
    NMES and BFR, Standard physical therapy
    Where
    United States
    Volunteers
    20 people
    Sponsor
    Stanford University
    Can I take part? ACL
  • Stroke Recurrence, Myocardial Infarction

    Cilostazol for Prevention of Recurrent Stroke Trial

    • Not yet recruiting
    • Age: 40 years and older
    • Phase 3
    • Pill or oral medicine

    The goal of this clinical study is to learn if adding a medicine called cilostazol to usual treatment can help prevent another stroke, a heart attack, or death in patients who had a stroke caused by a blocked blood vessel, or a…

    Conditions
    Stroke Recurrence, Myocardial Infarction, Vascular Death, Ischemic Stroke
    Trial name
    Clarity (NCT07174414)
    Testing
    Cilostazol 100 mg Tablets
    Where
    46 sites in United States
    Volunteers
    2,000 people
    Sponsor
    Stanford University
    Can I take part? Clarity
  • Alcohol Misuse

    Advancing Scalable Alcohol Brief Interventions in the ED: A Trial of Conversational AI With Digital Reinforcements

    • Recruiting
    • Age: 18 to 65 years
    • Lifestyle or therapy programme

    The goal of this clinical trial is to learn if a novel digital strategy combining a generative AI counseling agent (MICA) and weekly SMS boosters works to reduce risky drinking among Emergency Department patients.

    Trial name
    MICA-ED (NCT07661563)
    Testing
    MICA, TRAC
    Where
    United States
    Volunteers
    750 people
    Sponsor
    Stanford University
    Can I take part? MICA-ED
  • Acute Myeloid Leukemia (AML)

    Niclosamide in Pediatric Patients With Relapsed and Refractory AML

    • Recruiting
    • Age: 2 to 30 years
    • Phase 1
    • Pill or oral medicine

    Protocol is designed to evaluate a niclosamide dose escalation scale in combination with cytarabine as a therapeutic modality for pediatric subjects with relapsed/refractory acute myeloid leukemia.

    Trial name
    NCT05188170
    Testing
    Niclosamide
    Where
    United States
    Volunteers
    16 people
    Sponsor
    Stanford University
    Can I take part? NCT05188170

Completed, with results posted

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