Clinical trials: sponsored by Indiana University
Pregnancy Related
Medications in Breast Milk: A Convenience Pharmacokinetic Study
The benefits of breastfeeding and human milk consumption by infants has been clearly demonstrated. Benefits to the infant include reduction of infant and childhood diseases and allergies.
- Trial name
- MedMilk (NCT05099484)
- Testing
- The MedMilk study
- Where
- United States
- Volunteers
- 30 people
- Sponsor
- Indiana University
Type2 Diabetes, Depression
Program ACTIVE II: Behavioral Depression Treatment for Type 2 Diabetes
Program ACTIVE II is a depression treatment study sponsored by the National Institutes of Health, Indiana University, Ohio University and West Virginia University.
- Trial name
- NCT03371940
- Testing
- Program ACTIVE Exercise, Program ACTIVE CBT, Program ACTIVE
- Where
- 3 sites in United States
- Volunteers
- 140 people
- Sponsor
- Indiana University
Chronic Pain
Chronic Pain OneSheet Clinical Trial
The purpose of the study is to determine whether and how having access to the Chronic Pain OneSheet clinical decision support tool in Epic affects the ordering, prescribing, goal-setting, risk monitoring, and outcome measuring…
- Trial name
- NCT04295135
- Testing
- Chronic Pain OneSheet
- Where
- 2 sites in United States
- Volunteers
- 137 people, healthy volunteers welcome
- Sponsor
- Indiana University
Lower Limb Amputation
Development of Adaptive Vacuum Suspension to Improve Prosthetic Fit and Residual Limb Health
The purpose of the study is to evaluate residual limb circulation and skin health associated with the use of a prosthetic vacuum socket. A conventional non-vacuum prosthetic socket will be compared to a vacuum prosthetic socket.
- Trial name
- DoD (NCT03927404)
- Testing
- Active vacuum test prosthesis
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- Indiana University
Ostomy
Different Levels of Patient Education for Care of Ostomy Site
This is a randomized study of standard versus extra ostomy education.
- Trial name
- NCT02036268
- Testing
- Standard, Pre-operative Education, Two-week Post Operative Education
- Where
- United States
- Volunteers
- 53 people
- Sponsor
- Indiana University
Lymphoma, T-Cell, Cutaneous, Mycosis Fungoides
Biodynamic Imaging Utility in Predicting Response to Gemcitabine Chemotherapy in Mycosis Fungoides
This is a single-arm, non-randomized feasibility study designed to find out if the laser light-based imaging test called Biodynamic imaging (BDI) can correctly predict the cutaneous T-cell lymphoma mycosis fungoides (MF) cancer…
- Trial name
- BDI (NCT03789864)
- Testing
- Biodynamic imaging (BDI) of mycosis fungoides
- Where
- United States
- Volunteers
- 1 people
- Sponsor
- Indiana University
Stroke, CVA
Acute Effects of Beetroot Juice on Locomotor Economy and Capacity in Chronic Stroke
The purpose of this study is to investigate if a beetroot juice supplement can improve oxygen capacity during walking tasks at a submaximal and maximal effort in people greater than 6 months following stroke.
- Trial name
- NCT05720013
- Testing
- Beetroot Juice supplement
- Where
- United States
- Volunteers
- 22 people
- Sponsor
- Indiana University
Adolescent Behavior, Child Behavior
Sankofa Paradigm: A Therapeutic Theatre Program for Girls
The purpose of this study is to test the impact of a 6-week theatre intervention rooted in African culture (Sankofa) on the wellness of girls (predominately African American) ages 8-18 receiving services at five Boys \& Girls…
- Conditions
- Adolescent Behavior, Child Behavior, Mental Health Wellness 1, Mental Health Wellness 2
- Trial name
- NCT04518397
- Testing
- Theatre
- Where
- United States
- Volunteers
- 163 people
- Sponsor
- Indiana University
Traumatic Brain Injury, Alexithymia
Training to Reconnect With Emotional Awareness Therapy
To decrease emotional self-awareness deficits and improve emotional self-regulation, particularly anxiety, anger, depression, and positive affect, through the treatment of alexithymia.
- Trial name
- TREAT (NCT03414463)
- Testing
- TREAT
- Where
- United States
- Volunteers
- 44 people
- Sponsor
- Indiana University
Depression, Anxiety
Behavioral Activation in Depressed Online Workers
In this study, the investigators will test the effectiveness of a digital, low intensity mental health intervention in depressed individuals.
- Trial name
- BA-Prol (NCT06181825)
- Testing
- COMET-BA (Common Elements Toolbox- Behavioral Activation)
- Where
- United States
- Volunteers
- 804 people
- Sponsor
- Indiana University
Anxiety, Chemotherapy-induced Nausea and Vomiting
Use of Aromatherapy to Reduce Symptom Burden
The purpose of this study is to evaluate the effect of inhaled aromatherapy on symptoms of nausea/vomiting and anxiety in patients who have received a stem cell transplant.
- Trial name
- NCT05251337
- Testing
- Essential oils
- Where
- United States
- Volunteers
- 92 people
- Sponsor
- Indiana University
Symptomatic Irreversible Pulpitis
Buffered vs. Unbuffered Local Anesthesia in Mandibular Molars Diagnosed With Symptomatic Irreversible Pulpitis
The purpose of this study is to determine whether one type of anesthetic (numbing medicine) will work better at numbing the nerve in a tooth than using a different type of anesthetic.
- Trial name
- NCT05227300
- Testing
- Onset Sodium Bicarbonate Inj., 8.4%, USP Neutralizing Additive Solution, 2% lidocaine with 1:100,000 epinephrine
- Where
- United States
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Indiana University
Human Papilloma Virus Vaccine Hesitancy
HPV Vaccine Hesitancy Among Indiana Youth With Cancer and Blood Diseases
For the identified groups of patients (survivors of childhood cancer and youth with sickle cell disease) the investigators want to better understand the barriers to, and facilitators of, HPV vaccination.
- Trial name
- NCT04667702
- Testing
- Interviews
- Where
- United States
- Volunteers
- 176 people
- Sponsor
- Indiana University
Depression, Anxiety
Low-intensity Stepped Care for Internalizing Distress
The purpose of this study is to test the feasibility and efficacy of combining a single session intervention, COMET, with a self-help intervention, Doing what matters in times of stress. In step I, all individuals receive COMET.
- Conditions
- Depression, Anxiety, Emotion Regulation
- Trial name
- COMET-DWM (NCT05441111)
- Testing
- Common Elements Toolbox, Doing What Matters in Times of Stress: An Illustrated Guide, Guided self-help
- Where
- United States
- Volunteers
- 275 people
- Sponsor
- Indiana University
Traumatic Brain Injury (TBI)
Locomotor Recovery Following Traumatic Brain Injury
The purpose of this study is to investigate the effectiveness of two different walking training interventions on the recovery of strength, mobility, walking and other measures of health in individuals following traumatic brain…
- Trial name
- TBI_IU (NCT04503473)
- Testing
- High Intensity Stepping Training, Conventional Therapy
- Where
- United States
- Volunteers
- 17 people
- Sponsor
- Indiana University
IBS - Irritable Bowel Syndrome, Constipation
Efficacy of Psychological Therapies in Patients With Functional Bowel Disorders
The purpose of this study is study bowel symptoms, quality of life, and personal factors that may affect your health. In Aim 1 of this study participants will be invited to complete 6 survey-based questionnaires online.
- Trial name
- PTSD (NCT04060121)
- Where
- United States
- Volunteers
- 126 people
- Sponsor
- Indiana University
IBS
Fecal Metabolome and the Intestinal Microbiota in Irritable Bowel Syndrome
The purpose of this study is to find out the relationship between the bile acids, fatty acids (fatty acids are part of the diet) and bacteria that are present in the intestines.
- Trial name
- IBS (NCT02981888)
- Testing
- X-Ray
- Where
- United States
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Indiana University
Bone Marrow Transplant Complications, Acute Myeloid Leukemia
High-Dose Post-Transplant Cyclophosphamide, Bortezomib, and Sitagliptin for the Prevention of GVHD
This is an open label Phase I-II study to determine the safe doses of bortezomib, sitagliptin, and PTCy (Phase I) with expansion into a phase II trial to determine efficacy in improving survival.
- Conditions
- Bone Marrow Transplant Complications, Acute Myeloid Leukemia, Acute Lymphoblastic Leukemia, Adult, Myelodysplastic Syndromes
- Trial name
- NCT05895201
- Testing
- Sitagliptin, Bortezomib, Cyclophosphamide
- Where
- United States
- Sponsor
- Indiana University
Wound, Bacterial Infections
Biofilm Modified Macrophage Phenotype and Function in Diabetic Wound Healing
The purpose of this study is to learn more about biofilm and to see how it affects diabetic wounds. A biofilm can occur if a chronic infection causes bacteria to grow in a slime enclosed group.
- Conditions
- Wound, Bacterial Infections, Diabetes Mellitus, Infected Ulcer of Skin
- Trial name
- NCT03271580
- Testing
- Finger prick test for HbA1c measurement, Punch Biopsy, Vac Sponge Collection
- Where
- 5 sites in United States
- Volunteers
- 31 people
- Sponsor
- Indiana University
Diabetes Mellitus, Foot Ulcer
miR-200b & miR-21 in Diabetic Wounds
This study aims to determine if elevated wound-edge endothelial miR-200b is a barrier to wound healing in diabetic patients and also to determine if ex vivo supplementation of miR-21 mimic and recombinant MFG-E8 resolve…
- Conditions
- Diabetes Mellitus, Foot Ulcer, Ulcer, Diabetic Foot Ulcer
- Trial name
- NCT02581098
- Testing
- No interventions
- Where
- 4 sites in United States
- Volunteers
- 98 people
- Sponsor
- Indiana University
The first 1,020 results can be paged through. Add a filter or change the sort order to reach the rest.