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NCT02588027 · ClinicalTrials.gov registry record · NA
Effect of Ibuprofen on Postoperative Opiate Medication Use and Shoulder Functional Outcomes
A NA study of Rotator Cuff Tear Arthropathy, sponsored by University of California, San Francisco.
- Completed
- Registry status
- NA
- Development phase
- 110
- Enrollment target
- 1
- Study location
NCT02588027: Completed NA study of Rotator Cuff Tear Arthropathy, sponsored by University of California, San Francisco.
NCT02588027 is a NA study of Rotator Cuff Tear Arthropathy that has completed, run by University of California, San Francisco. The registered enrollment target is 110 participants, below the 3,444-participant average among 6 other Rotator Cuff Tear Arthropathy trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02588027, a NA study of Rotator Cuff Tear Arthropathy, has completed, sponsored by University of California, San Francisco.
- COMPLETED
- Registry status
- NA
- Development phase
- 110 participants
- Enrollment target
- 1
- Study location
Study Summary
This will be a randomized controlled trial to determine if postoperative ibuprofen after arthroscopic rotator cuff repair impacts postoperative opiate medication use, Visual Analog Scale (VAS) pain scores, shoulder range of motion (ROM), and repair integrity.
Primary Outcome
pain control
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Ibuprofen
Study Locations (1)
California
- UCSF Orthopaedic Institute - San Francisco
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 110 participants |
| Start Date | 2015-10 |
| Est. Completion | 2022-09 |
| Phase | NA |
What the finished NCT02588027 record still lists
NCT02588027 is an interventional study that assigns participants to a tested intervention. The registered 110 participants enrollment target is mid-sized for trials with a published cap, below the 3,444-participant average among 6 other Rotator Cuff Tear Arthropathy trials with a reported enrollment target (97% lower).
The record links to 1 condition, with Rotator Cuff Tear Arthropathy appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT02588027 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT02588027 about?
NCT02588027 is a clinical study titled "Effect of Ibuprofen on Postoperative Opiate Medication Use and Shoulder Functional Outcomes". This will be a randomized controlled trial to determine if postoperative ibuprofen after arthroscopic rotator cuff repair impacts postoperative opiate medication use, Visual Analog Scale (VAS) pain scores, shoulder range of motion (ROM), and repair integrity.
What is the current status of trial NCT02588027?
This trial is currently completed. It is a NA study. The enrollment target is 110 participants. The study started on 2015-10. Estimated completion is 2022-09.
What conditions does trial NCT02588027 study?
This clinical trial studies the following conditions: Rotator Cuff Tear Arthropathy.
What interventions are being tested in trial NCT02588027?
The interventions under investigation include: Placebo (DRUG), Ibuprofen (DRUG).
Who is sponsoring clinical trial NCT02588027?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02588027 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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