Clinical trials

13

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
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Status: Not yet recruiting

Effects of Caffeine on Chess Performance and Cognitive Function in Professional Chess Players

This study will examine whether caffeine improves cognitive and competitive performance in professional chess players during tournament-style games. In a randomized double-blind crossover design, participants will complete two experimental sessions in which they consume either caffeinated coffee or decaffeinated coffee before playing a standardized chess match. Cognitive performance will be assessed using attention and reaction-time tests, including the Stroop Test, Trail Making Test, and Puzzle Rush task. Chess performance outcomes such as move accuracy, time management, and error rates will also be evaluated. The study aims to determine whether moderate caffeine intake enhances focus, alertness, and decision-making during prolonged competitive chess play.

Participants needed: 12
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: St. Louis UniversityUpdated: Jun 11, 2026Locations: 1
Eligibility criteria

Male and female professional chess players aged 18-50 years [+4]

Non-caffeine users [+11]

Status: Recruiting

Testosterone Treatment in Men With Chronic Kidney Disease

This study in being conducted in men who have low testosterone and chronic kidney disease. The investigators will evaluate the effects of an oral testosterone preparation, JATENZO, on testosterone levels and hemoglobin (red blood cells).

Participants needed: 20
Trial details
Phase: Phase 2Age: 18-85Biological sex: MaleType: InterventionalSponsor: St. Louis UniversityUpdated: Apr 30, 2026Locations: 1
Eligibility criteria

Men between ages of 18-85 years of age [+4]

Use of TRT currently or in the past 6 months, including use of over-the-counter... [+15]

Status: Recruiting

Post-Op Pain Control for Prophylactic Intramedullary Nailing.

Nationally, the opioid crisis has become a major epidemic with increasing mortality rates each year. Orthopedic surgeons routinely prescribe narcotics instead of NSAIDs for post-op pain control because of risk of delayed healing and nonunion due to NSAID use. Orthopedic oncology, however, has a unique subset of patients that undergo prophylactic placement of intramedullary femoral nails. Because no fracture is present, these patients do not rely on inflammatory healing factors, allowing for post-op NSAID use. This study sets out to determine the effect of post-op toradol use in addition to opioids compared to solely opioids in patients undergoing prophylactic nailing of the femur.

Participants needed: 60
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: St. Louis UniversityUpdated: Apr 22, 2026Locations: 1
Eligibility criteria

Femoral Shaft or Neck bone lesion [+2]

Concurrent pathologic fracture [+15]

Status: Recruiting

Local Bisphosphonate Effect on Recurrence Rate in Extremity Giant Cell Tumor of Bone

The purpose of the clinical study is to investigate whether the local delivery of bisphosphonate as a surgical adjuvant can decrease the chance of a giant cell tumor of bone coming back to the same location. The hypothesis is that the local administration of bisphosphonate will decrease the rate of the tumor returning compared to traditional aggressive surgical removal of the tumor.

Participants needed: 120
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: St. Louis UniversityUpdated: Apr 22, 2026Locations: 16
Eligibility criteria

Primary benign GCT of bone [+3]

Recurrent GCT of bone [+4]

Status: Recruiting

Reduction of Bacterial Seeding in Total Shoulder Arthroplasty

The purpose of this study is to compare the growth of intra-operative tissue cultures of Cutibacterium Acnes after primary shoulder replacement when using a no-prep control group versus Prontosan wound gel applied to the skin layer after the skin incision has been made.

Participants needed: 60
Trial details
Age: 18+Biological sex: MaleType: InterventionalSponsor: St. Louis UniversityUpdated: Mar 10, 2026Locations: 1
Eligibility criteria

Adult male 18 years of age or older undergoing elective primary total shoulder a...

Any revision shoulder arthroplasty procedure or other shoulder surgery that is n... [+4]

Status: Recruiting

Efficacy of Methylprednisolone for Pain Control After ACL Repair

Opioids are commonly used after orthopedic surgery for pain control but have been shown to increase complications, surgeries, readmissions, and risk for opioid use disorder. The purpose of this study is to investigate the impact of adding a methylprednisolone taper to the pain regimen after ACL repair surgery to determine if this results in decreased postoperative pain and opioid use without increasing complications.

Participants needed: 90
Trial details
Phase: Phase 4Age: 13-50Biological sex: AllType: InterventionalSponsor: St. Louis UniversityUpdated: Oct 24, 2025Locations: 1
Eligibility criteria

Patient undergoing ACL repair or ACL reconstruction with tendon autograft [+2]

Concurrent and significant injury to other bones or organs (Injury Severity Scor... [+8]

Status: Recruiting

MAP for Coaches: Translating Sports Injury Prevention Knowledge to Youth Sport Coaches

The goal of this clinical trial is to test the effectiveness of the MAP for Coaches, a web-based Musculoskeletal Athletic injury Prevention training course, in youth sport coaches. The main question it aims to answer are: * Is the MAP for Coaches effective in increasing coaches' sport-specific knowledge of musculoskeletal injuries (types, incidence, risk factors, mechanisms, and best prevention practices, with focus on neuromuscular training warm-up exercise programs)? * Is the MAP for Coaches effective in increasing coaches' motivation (self-efficacy and intention) to use sport-specific neuromuscular training warm-up exercise programs? The additional questions it aims to answer are: * Are the effects of the MAP for Coaches sustained in the short- and long-term? * Is the MAP for Coaches effective in promoting the use of sport-specific neuromuscular training warm-up exercise programs in youth sport coaches? Regardless of group, participants will receive the MAP for Coaches eLearning training course; however, the participants allocated to the control group will have their post-test survey completed right after they review the sport-specific 2-page injury prevention e-book containing an overview of the MAP for Coaches training course, including an infographic summary (Summarized MAP for Coaches eLearning Training Course). The intervention group will complete the post-test survey after the full training including both the course summary and the detailed course modules (the full training). The investigators will compare the two groups to see if an exposure to the (Full) MAP for Coaches eLearning Training Course improves study outcomes compared with the control group.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: St. Louis UniversityUpdated: Oct 2, 2025Locations: 1
Eligibility criteria

Active and ongoing engagement in team youth sport coaching [+2]

Additional engagement in adult coaching [+1]

Status: Recruiting

Mindfulness in Endometrial and Cervical Cancer

Patients with endometrial cancer who will be undergoing surgery or patients with cervical cancer who will be treated with chemoradiation will be randomized to utilize the Headspace smartphone application or not prior to their anticipated treatment.

Participants needed: 120
Trial details
Age: 18-90Biological sex: FemaleType: InterventionalSponsor: St. Louis UniversityUpdated: Sep 30, 2025Locations: 1
Eligibility criteria

New diagnosis of either 1) endometrial cancer undergoing surgery or 2) cervical... [+1]

Non-English speaking [+2]

Status: Recruiting

Short-term Effects of Caffeine and a Multi-ingredient Pre-workout on Exercise Performance

The investigators are conducting a study to see how a commercial pre-workout supplement, coffee, and water affect how well people perform. The study is conducted across four visits. The first visit is to assess the participants, and the next three visits are for testing. Each participant will drink a randomly assigned beverage 45 minutes before testing. Throughout the study, the participants will complete three testing days-each at least three days apart-so they can try all three drinks. The first test is the Wingate test, where the participants pedal as fast as they can for 30 seconds against a set resistance. The second test is a 1-mile treadmill run/walk on an incline, where the participant tries to complete the distance as fast as possible. The third test measures reaction time using light-up buttons to see how quickly a participant responds by touching them. These tests will help determine if any of the drinks improve performance. The results can help people choose the best drink for their workouts or races.

Participants needed: 12
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: St. Louis UniversityUpdated: Aug 19, 2025Locations: 1
Eligibility criteria

Are a healthy male or female adult aged 18-35 years old [+2]

Have a history of or currently have a cardiovascular or metabolic disease (e.g.,... [+7]

Status: Recruiting

Preconception Intervention for Incarcerated Women With Substance Use

The goal of this pilot trial is to test the feasibility and acceptability as well as efficacy of the adapted intervention, CHOICES-PLEAS (Pregnancy Liberated from Exposure to Alcohol and Substances) among women will illicit polysubstance use participating in a court-mandated jail-based 90-day substance use disorder treatment program. The main questions it aims to answer are: 1. What is the feasibility and acceptability of implementing the CHOICES-PLEAS intervention in a court-mandated jail-based substance use disorder treatment program? 2. Does participation in CHOICES-PLEAS lower the risk of a substance exposed pregnancy at 1 and 3 months after release compared to a control condition? 3. Does participation in CHOICES-PLEAS increase motivation to change substance use and reduce risky sexual behaviors at 1 and 3 months after release compared to a control condition? Participants will receive three one-on-one motivational interviewing sessions and one family planning referral visit during incarceration and one booster session at 1 month after release from jail. Researchers will compare the CHOICES-PLEAS intervention to a control condition to see if participation in the intervention reduces risk of substance exposed pregnancy, increases motivation to change substance use, and reduces risk of risky sexual behaviors.

Participants needed: 90
Trial details
Age: 18-49Biological sex: FemaleType: InterventionalSponsor: St. Louis UniversityUpdated: Jul 22, 2025Locations: 1
Eligibility criteria

English-speaking [+4]

Participated in a focus group that was part of the formative work for this study... [+4]

Status: Recruiting

Step Up to PD: A Community-based Walking Program for People With Parkinson's Disease

This study will investigate the feasibility of a 6-month community walking program for people with Parkinson's disease (PD) and their care partners in greater Saint Louis, Missouri region. The walking program will consist of weekly, organized walking groups at the Missouri Botanical Gardens. Participants in the program will use Nordic walking poles during the walks. The walking group(s) will meet once per week and will be supervised by walking group leaders from Saint Louis University. Participants will be given a smart watch to wear that will help step counts will be tracked in real-time. The program is designed to get people with Parkinson's disease out of their homes, cultivate a culture of connection with others with Parkinson's disease, and to be collectively accountable for a common goal toward increasing their physical and social engagement in their communities.

Participants needed: 40
Trial details
Age: 30-85Biological sex: AllType: InterventionalSponsor: St. Louis UniversityUpdated: May 14, 2025Locations: 1
Eligibility criteria

30-85 years old [+3]

Health diagnosis that would limit exercise participation (e.g., heart problems,... [+3]

Status: Recruiting

APOL1 Genetic Testing in African Americans

Recent breakthroughs in medical genetics have discovered that a portion of kidney failure affecting the Black community is mediated by coding variants in a gene called apolipoprotein L1 (APOL1) - and that genetic variants, not race - account for increased risk. For APOL1 genetic testing to be applied in a manner that improves patient care and outcomes, more information is needed regarding associations of genotype with clinical parameters related to kidney health. Further, understanding patient perceptions about knowledge of the results of APOL1 genetic testing, and how that impacts patient engagement with management of hypertension and other renal risk factors, is urgently needed. * In a Phase 1 pilot study, we offered APOL1 genetic testing to Black patients seen in our Hypertension and Nephrology clinics at Saint Louis University, an academic medical center that serves the local urban community, and surveyed patients on attitudes and concerns about APOL1 genetic testing. 144 participants were enrolled in Phase 1. * In the Phase 2 study, we will advance this important work in our community by offering participation to a broader patient base, including patients seen in Internal and Family Medicine clinics, SLU Hospital, as well as to first-degree relatives and spouses of SLUCare participants. This expansion seeks to advance understanding of environment-gene interactions, improve risk prediction, and target management of potentially modifiable risk factors.

Participants needed: 600
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: St. Louis UniversityUpdated: Mar 20, 2025Locations: 1
Eligibility criteria

Ages 18-90 [+1]

Cognitively impaired/unable to provide consent [+2]

Status: Recruiting

Vertebral Artery Origin Treatment Via Endovascular Techniques Registry (VOTER)

A retrospective and prospective registry of patients admitted for stroke and evidence of Vertebral Artery Origin Stenosis (VAOS).

Participants needed: 150
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: St. Louis UniversityUpdated: Feb 12, 2025Locations: 10Duration: 1 Year
Eligibility criteria

Patients between 18 and 90 years of age [+3]

Pregnant women [+5]