Clinical trials: sponsored by University of Utah
Intertrochanteric Femur Fracture, Muscle Atrophy
Intertrochanteric Femur Fracture Patients Who Receive Metformin With a Placebo
The investigators central hypothesis is that metformin supplementation will be well-tolerated, safe, and provide patients with improved functional and muscle morphology outcomes following intertrochanteric femur fracture.
- Trial name
- NCT07179042
- Testing
- Metformin
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- University of Utah
Intraarticular Fracture and Post-traumatic Osteoarthritis
Inflammatory Response Following Intraarticular Fracture
The purpose of the study is to investigate a relationship between the inflammatory response following intraarticular fracture and post-traumatic osteoarthritis.
- Trial name
- PTOA (NCT01514643)
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- University of Utah
Ankle Fractures
Local Multimodal Injection Versus Regional Anesthesia in Controlling Pain for Treating Rotational Ankle Fractures
The investigators plan to evaluate the efficacy in reducing post-operative pain between local multimodal analgesia as compared to regional anesthesia in rotational ankle fractures.
- Trial name
- NCT05019638
- Testing
- Regional anesthesia group, Local multimodal analgesia group
- Where
- 2 sites in United States
- Volunteers
- 200 people
- Sponsor
- University of Utah
Dementia, Hearing Loss
Evaluation of the Impact of Cochlear Implants on Cognition in Older Adults
The subjects will be age 65 years and older, with no upper limit of age range with hearing loss that are candidates for standard-of-care cochlear implant.
- Conditions
- Dementia, Hearing Loss, Presbycusis
- Trial name
- NCT02729402
- Testing
- Cognitive Testing
- Volunteers
- 37 people, healthy volunteers welcome
- Sponsor
- University of Utah
Cancer
Improving Health Insurance Literacy Among Young Adult Cancer Survivors
We will conduct a randomized controlled trial to test a 4-session virtual health insurance navigation intervention that will increase knowledge about health insurance, reduce financial burden, and improve surveillance for…
- Trial name
- CHAT-S (NCT05829070)
- Testing
- CHAT-S, Usual Care
- Where
- 2 sites in United States
- Volunteers
- 300 people
- Sponsor
- University of Utah
Coagulation Disorder, Blood
The Effectiveness of a Novel Software Program to Help in ROTEM Interpretation
The purpose of this study is to assess a novel rotational thromboelastometry (ROTEM®) interpretation software to determine whether its use improves the accuracy of clinician interpretation.
- Trial name
- NCT05591014
- Testing
- Novel ROTEM interpretation software
- Where
- United States
- Volunteers
- 26 people
- Sponsor
- University of Utah
Body Weight Changes, Athletic Performance
Whey Protein Supplementation in High School Athletes
The overall aim of this project is to compare protein supplementation on performance, recovery, and body composition changes in adolescent soccer players between the whey protein and the control group in response to the…
- Conditions
- Body Weight Changes, Athletic Performance, Recovery, Sleep
- Trial name
- NCT05589129
- Testing
- Whey Protein Supplement
- Where
- United States
- Volunteers
- 31 people, healthy volunteers welcome
- Sponsor
- University of Utah
Trigger Point Pain, Myofascial
Accuracy of Rib Palpation for Dry Needling of Deep Periscapular Musculature, Measured With Ultrasound
Ultrasound was used to identify the location of a rib. This was compared to a practitioner's ability to palpate the area.
- Trial name
- NCT04066166
- Testing
- Palpation
- Volunteers
- 44 people, healthy volunteers welcome
- Sponsor
- University of Utah
Weber B Ankle Fractures
Analysis of Medial Clear Space Widening in Weber B Ankle Fractures
The investigators purpose of this study is to obtain all three standard of care stress views of the ankle (gravity stress, manual stress, weightbearing stress) to compare the amount of tibiotalar joint instability predicted by…
- Trial name
- NCT07028944
- Testing
- Gravity assisted stress, Manual external rotation stress, Weight-bearing stress
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- University of Utah
Distal Radius Fractures
Hematoma Block Versus Bier Block for Closed Fracture Reduction
The investigators objective of this study is to evaluate the effectiveness of hematoma block versus intravenous regional anesthesia (Bier block) during closed reduction of distal radius fractures.
- Trial name
- NCT05086224
- Testing
- Hematoma Local Anesthetic Block Procedure with 1% Lidocaine, Bier Anesthetic Block Procedure with 1% Lidocaine
- Where
- United States
- Volunteers
- 500 people
- Sponsor
- University of Utah
Pain
Cannulated Bone Bolt® Screw System Versus Standard Cannulated Screw System Fixation for Pelvic Fractures
The investigators aim is to determine if the cannulated Bone Bolt® screw system will provide improved post-operative pain control as compared to standard cannulated screw system fixation for the operative treatment of LC1…
- Trial name
- NCT07209280
- Testing
- Cannulated Bone Bolt® Screw System, Standard Cannulated Screw System
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- University of Utah
Pseudarthrosis After Fusion or Arthrodesis
Collecting Bone Graft During Spinal Decompression and Posterolateral Lumbar Fusion to Better Define Bone Making Cells
The purpose of this study is to improve fusion (bony healing) techniques and improve patient recovery by identifying cells in your body that make bone.
- Trial name
- NCT01409954
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- University of Utah
Cervical Myelopathy
Activity Monitors as a Measure of Physical Function in Degenerative Cervical Myelopathy
The investigators objective of this research is to compare activity monitor results with standard of care (SOC) question-based outcome measures for degenerative cervical myelopathy patients before and after treatment with…
- Trial name
- NCT04498806
- Testing
- Fitbit
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- University of Utah
Hearing Impairment
CROS and Quality of Life of Elderly Cochlear Implant Recipients and Their Care Givers
The purpose of this study is to assess the effect of the Naida Link contralateral routing of signal (CROS) device on speech understanding in challenging listening situations and on the quality of life in unilateral CI recipients…
- Trial name
- NCT04794179
- Testing
- Naida Link CROS
- Where
- United States
- Volunteers
- 16 people
- Sponsor
- University of Utah
Inflammatory Bowel Diseases, Contraception
Hormonal Influences on Inflammatory Bowel Diseases
Of the 1.8 million females with inflammatory bowel diseases (IBD) in the US, over half of those who are premenopausal suffer from cyclical menstrual-related IBD symptoms, regardless of how well their disease is controlled.
- Conditions
- Inflammatory Bowel Diseases, Contraception, Menstrual Problem
- Trial name
- NCT05610527
- Testing
- Proposed study design and randomization scenarios, Repeated measures of validated Inflammatory Bowel Disease Patient Reported Outcome Instruments, Inflammatory marker collection and assessment for correlation with PRO responses and menstrual timing
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- University of Utah
Abortion Early
Atorvastatin as a Potential Adjunct to Misoprostol for Termination of Pregnancy
Medication abortion is a way of ending a pregnancy using pills. The current FDA-approved regimen for medication abortion uses mifepristone and misoprostol.
- Trial name
- NCT05342974
- Testing
- Atorvastatin, Misoprostol
- Where
- United States
- Volunteers
- 9 people, healthy volunteers welcome
- Sponsor
- University of Utah
Contraception
Levonorgestrel 52 mg IUD for Emergency Contraception and Same-Day Start
This is a prospective clinical research study to test the effectiveness of the Levonorgestrel (LNG) 52 mg Intrauterine Device (IUD) for emergency contraception (EC) and same-day start use that will enroll people receiving care at…
- Trial name
- NCT05444582
- Testing
- Levonorgestrel 52 MG Intrauterine System
- Where
- 8 sites in United States
- Volunteers
- 1,404 people
- Sponsor
- University of Utah
Placenta Accreta
Use of ROTEM Intraoperatively in Women With Placenta Accreta
This study evaluates the use of rapid tests for hematocrit and clotting function in women undergoing surgery for placenta accreta.
- Trial name
- ROTEM (NCT02729974)
- Testing
- ROTEM, standard treatment
- Volunteers
- 32 people
- Sponsor
- University of Utah
Placenta Accreta
Conservative Management for PAS Pilot
Conservative in situ management is a promising alternative treatment to hysterectomy for patients with placenta accreta spectrum and may be safer and preferable for some patients.
- Trial name
- NCT05139498
- Testing
- Conservative management for placenta accreta spectrum (PAS), Cesarean hysterectomy for placenta accreta spectrum (PAS)
- Where
- United States
- Volunteers
- 4 people
- Sponsor
- University of Utah
Lung Cancer
UG3 Pilot Clinical Trial
LungSMART Utah utilizes a Population Health Management (PHM) approach that addresses key barriers to Lung Cancer Screening (LCS) implementation by deploying a centralized Hub infrastructure for eligibility assessment…
- Trial name
- NCT07073898
- Testing
- Repeated Text Messages (TM+), Conversational Agent (CA), Educational Video
- Where
- United States
- Volunteers
- 65 people
- Sponsor
- University of Utah