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NCT06381791 · ClinicalTrials.gov registry record · Phase 1
CBD for Pain Following Orthopedic Shoulder Surgery
A Phase 1 study of Rotator Cuff Injuries and Shoulder Osteoarthritis, sponsored by The Methodist Hospital Research Institute.
- Recruiting
- Registry status
- Phase 1
- Development phase
- 80
- Enrollment target
- 1
- Study location
NCT06381791 is a Phase 1 study of Rotator Cuff Injuries and Shoulder Osteoarthritis that is actively recruiting participants, run by The Methodist Hospital Research Institute. The registered enrollment target is 80 participants, below the 93-participant average among 10 other Rotator Cuff Injuries trials with a reported enrollment target (14% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06381791, a Phase 1 study of Rotator Cuff Injuries and Shoulder Osteoarthritis, is actively recruiting participants, sponsored by The Methodist Hospital Research Institute.
- RECRUITING
- Registry status
- Phase 1
- Development phase
- 80 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of the study is to learn if Epidiolex (cannabidiol) works as a additional pain medication in patients who have had orthopedic shoulder surgery. It is also to learn about safe dosages and identify any side effects after surgery. Researchers will compare Epidiolex to a placebo solution to see if Epidiolex lowers pain after shoulder surgery. Participants will: * track their pain and what medications they use every day in a provided pain diary. A researchers will call every seven days to check on the participant and diary. * Complete two short surveys. Once before surgery and once after. * Have bloodwork tested after surgery
Conditions Studied
Interventions
- DRUG Epidiolex
- DRUG Placebo oral solution
Study Locations (1)
Texas
- Houston Methodist Hospital - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2024-05-24 |
| Est. Completion | 2027-12-30 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06381791
The ClinicalTrials.gov registry entry for NCT06381791 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 93-participant average among 10 other Rotator Cuff Injuries trials with a reported enrollment target (14% lower). The listed sponsor is The Methodist Hospital Research Institute, which has 126 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Rotator Cuff Injuries appearing as the primary indexed condition, and to 2 interventions - of which Epidiolex is the first listed.
NCT06381791 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT06381791 about?
NCT06381791 is a clinical study titled "CBD for Pain Following Orthopedic Shoulder Surgery". The goal of the study is to learn if Epidiolex (cannabidiol) works as a additional pain medication in patients who have had orthopedic shoulder surgery. It is also to learn about safe dosages and identify any side effects after surgery. Researchers will compare Epidiolex to a placebo solution to se...
What is the current status of trial NCT06381791?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 80 participants. The study started on 2024-05-24. Estimated completion is 2027-12-30.
What conditions does trial NCT06381791 study?
This clinical trial studies the following conditions: Rotator Cuff Injuries, Shoulder Osteoarthritis.
What interventions are being tested in trial NCT06381791?
The interventions under investigation include: Epidiolex (DRUG), Placebo oral solution (DRUG).
Who is sponsoring clinical trial NCT06381791?
This trial is sponsored by The Methodist Hospital Research Institute, which has 126 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06381791 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.