Clinical trials: sponsored by Stanford University
Fuchs, Fuchs Dystrophy
Descemet Endothelial Thickness Comparison Trial II
Descemet Endothelial Thickness Comparison Trial (DETECT) II is a multi-center, outcome assessor-masked, placebo-controlled clinical trial randomizing 60 patients with Fuchs endothelial dystrophy to DMEK versus Descemet Stripping…
- Conditions
- Fuchs, Fuchs Dystrophy, Fuchs' Endothelial Dystrophy
- Trial name
- DETECT II (NCT05275972)
- Testing
- Ripasudil
- Where
- 8 sites in United States
- Volunteers
- 60 people
- Sponsor
- Stanford University
GVHD, Hematopoietic Cell Transplantation (HCT)
TACrolimus Targeted Immunosuppression Cessation in ALlogeneic HCT
The purpose of this study is to test the feasibility and safety of early cessation of tacrolimus following allogeneic hematopoietic cell transplantation (HCT).
- Conditions
- GVHD, Hematopoietic Cell Transplantation (HCT), Acute Myeloid Leukemia (AML), Myelodysplastic Syndromes
- Trial name
- NCT07302776
- Testing
- Tacrolimus, Early Tacrolimus Taper Strategy
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- Stanford University
Diet Quality, Young Adult Health
Young Adult Food Messaging Experiment
The primary objective of this study is to identify the food counter-marketing messages (i.e., messages that describe deceptive marketing tactics used by food companies) that are perceived as most effective among young adults.
- Conditions
- Diet Quality, Young Adult Health, Communication
- Trial name
- NCT07768462
- Testing
- Lying about unhealthy foods being healthy, Engineering foods to be addictive, Targeting groups
- Where
- United States
- Volunteers
- 645 people, healthy volunteers welcome
- Sponsor
- Stanford University
Fuchs
Descemet Endothelial Thickness Comparison Trial I
Descemet Endothelial Thickness Comparison Trial (DETECT) I is a multi-center, outcome assessor-masked, placebo-controlled clinical trial randomizing 160 patients in a 2x2 factorial design.
- Trial name
- DETECT I (NCT05289661)
- Testing
- Topical Ripasudil
- Where
- 7 sites in United States
- Volunteers
- 160 people
- Sponsor
- Stanford University
Ulnar Wrist Pain
Blood Flow Restriction for Ulnar Sided Wrist Pain
The purpose of this study is to determine the strength, pain and functional benefits of early, low-load resistance training with blood flow restriction (BFR) in ulnar-sided wrist pain treated nonoperatively with immobilization…
- Trial name
- NCT06963671
- Testing
- Blood Flow Restriction
- Where
- United States
- Volunteers
- 90 people
- Sponsor
- Stanford University
Healthy Controls
Reliability of [18F]-FTC-146 Brain Uptake in Healthy Controls
The purpose of this study is to understand the reliability of [18F]-FTC-146 brain uptake in healthy controls.
- Trial name
- rSIG (NCT03649555)
- Testing
- [18F]-FTC-146
- Where
- United States
- Volunteers
- 5 people, healthy volunteers welcome
- Sponsor
- Stanford University
Obsessive-Compulsive Disorder
Understanding How Ketamine Brings About Rapid Improvement in OCD
The purpose of this study is to understand how ketamine brings about rapid improvement in Obsessive-Compulsive Disorder (OCD) symptoms.
- Trial name
- MKET (NCT02624596)
- Testing
- Ketamine, Midazolam
- Where
- United States
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Stanford University
Obsessive Compulsive Disorder
Computerized Training for Individuals Diagnosed With Obsessive-Compulsive and Related Disorders
Obsessive-Compulsive Disorder (OCD) is a chronic and disabling disorder that costs the economy over $2 billion annually and represents a significant public health problem.
- Trial name
- EmRT (NCT03182075)
- Testing
- Computerized Training
- Where
- United States
- Volunteers
- 5 people
- Sponsor
- Stanford University
Hoarding Disorder
Neural Mechanisms of Decision Making in Hoarding Disorder
The purpose of this study is to understand the neural mechanisms of decision making in hoarding disorder.
- Trial name
- LOSS (NCT03487224)
- Testing
- MRI with fMRI frequency
- Where
- United States
- Volunteers
- 25 people, healthy volunteers welcome
- Sponsor
- Stanford University
OCD
Open/Aftercare Treatment for Participants Diagnosed With Obsessive Compulsive Disorder
The purpose of this study is to provide participants diagnosed with obsessive compulsive disorder (OCD) and completed one of the active study protocols at the Rodriguez Lab, with open/aftercare treatment.
- Trial name
- NCT03511534
- Testing
- Psychotherapy, Pharmacotherapy
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- Stanford University
Obsessive-Compulsive Disorder
ERP Plus Improv Group Therapy for OCD (IMPROVE Study)
The goal of this study is to pilot test a novel group therapy intervention for adults with OCD.
- Trial name
- NCT06265233
- Testing
- Group Improv sessions, Group Exposure and Response Prevention (ERP) Therapy
- Where
- United States
- Volunteers
- 7 people
- Sponsor
- Stanford University
Cancer, Lung Cancer
Biodistribution & Pharmacokinetic of Position Emission Tomography (PET) Radiopharmaceutical 18F C SNAT4
Primary Objectives Determine the biodistribution of [18F]-C-SNAT4 in 5 healthy volunteers. Secondary Objectives Determine the dosimetry of [18F]-C-SNAT4 PET in healthy volunteers and patients with lung cancer.
- Trial name
- NCT04017819
- Testing
- 18F-C-SNAT4, Positron emission tomography (PET)/Computed tomography (CT) Scan
- Where
- United States
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Stanford University
Follicular Lymphoma, Mantle Cell Lymphoma
AutologousCD22 Chimeric Antigen Receptor (CAR)T Cells in w/Recurrent/Refractory B Cell Lymphomas
This is a non-randomized clinical trial to evaluate the safety and efficacy of CD22CART administered after lymphodepleting chemotherapy in adults with relapsed / refractory B Cell Lymphomas.
- Conditions
- Follicular Lymphoma, Mantle Cell Lymphoma, Hairy Cell Leukemia, Lymphoplasmacytic Lymphoma
- Trial name
- NCT06340737
- Testing
- CD22CART Infusion
- Where
- United States
- Volunteers
- 148 people
- Sponsor
- Stanford University
Cancer Distress, Cancer Coping
Aromatherapy Inhaler Use for HSCT Distress
This randomized controlled trial will evaluate the feasibility and acceptability of an inhaled aromatherapy stick for patients during the acute inpatient phase after hematopoietic cell transplantation (HCT) .
- Conditions
- Cancer Distress, Cancer Coping, Hematopoetic Stem Cell Transplant, Aromatherapy
- Trial name
- NCT05302583
- Testing
- Aromatherapy Stick, Standard of Care
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- Stanford University
Adolescent Behavior, Pediatric Cancer
Feasibility Usability & Acceptability Study: Symptom Reporting by Children Adolescents & Young Adults w/Cancer
The purpose of this project is to pilot test an electronically delivered symptom assessment tool Pediatric Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (Ped-PRO-CTCAE), completed by…
- Conditions
- Adolescent Behavior, Pediatric Cancer, Oncology
- Trial name
- NCT06824441
- Testing
- Age- and Role-Specific Questionnaire Administration
- Where
- United States
- Volunteers
- 85 people
- Sponsor
- Stanford University
cGVHD
IL6-receptor Inhibitor Iwith Belumosudil for the Treatment of Belumosudil-refractory cGVHD
A single-center, Phase 1, open-label, investigator-initiated clinical trial evaluating the safety, tolerability, and preliminary efficacy of sarilumab (anti-IL-6R) monotherapy as a rescue in adult patients with…
- Trial name
- NCT07484113
- Testing
- Belumosudil, Sarilumab
- Volunteers
- 10 people
- Sponsor
- Stanford University
Gastroenteropancreatic Neuroendocrine Tumor
Study of PRRT in Metastatic, WHO Grade 1 or 2, SSTR Positive, GEP-NET Who Are Candidates for Cytoreductive Surgery
The purpose of this study is to learn about the feasibility and safety of using Peptide Receptor Radionuclide Therapy (PRRT) before and after surgical removal of a tumor.
- Trial name
- NCT04609592
- Testing
- Lutathera, Gallium 68 Dotatate, Computed Tomography (CT)
- Where
- United States
- Volunteers
- 10 people
- Sponsor
- Stanford University
Lymphedema, Breast Cancer, Lymphedema
LYMPHA Procedure for the Prevention of Lymphedema After Axillary Lymphadenectomy
Lymphedema is a chronic, progressive, and debilitating condition that occurs with disruption or obstruction of the lymphatic system, which commonly occurs a result of breast cancer therapy.
- Trial name
- NCT05366699
- Testing
- axillary lymphadenectomy with immediate lymphatic reconstruction (LYMPHA), Axillary lymphadenetomy alone, axillary lymphadenectomy with soft tissue reinforcement
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- Stanford University
Pregnancy, Pharmacokinetics
Pharmacokinetics of Oral Calcium Carbonate in Parturients
This study investigates the time course of change in calcium in the blood after a pregnant subject takes an oral dose of calcium carbonate (commonly marketed as "Tums").
- Conditions
- Pregnancy, Pharmacokinetics, Postpartum Hemorrhage
- Trial name
- NCT06650930
- Testing
- Oral calcium carbonate, Oral calcium citrate
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- Stanford University
Type 1 Diabetes Mellitus, Exercise Physiology
Using a Personalized Decision Support Tool to Help People With Type 1 Diabetes Manage Exercise
This study evaluates a clinician-facing decision-support toolkit designed to assist adults with type 1 diabetes in preparing for moderate-intensity exercise.
- Trial name
- NEXT (NCT07226583)
- Testing
- Standard-of-Care Guidance (SoC), Usual Care (UC), netIOB & Exercise Toolkit (NEXT)
- Where
- United States
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Stanford University
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