Nonopioid Pain Control After Labral Surgery
This study is comparing two ways to manage pain after labral surgery (surgery on the shoulder or hip joint). One group will receive a non-opioid pain regimen, which includes medications like Celecoxib, Ketorolac, Gabapentin, and Acetaminophen. The other group will receive the traditional pain control, which includes Hydrocodone-Acetaminophen (a narcotic). Researchers want to see if the non-opioid approach can reduce pain as effectively. You may be able to join if you are an adult over 18 and are scheduled for labral surgery. The study will measure your pain levels and how you feel about your recovery 10 days after surgery. The study aims to enroll 100 participants.
- Study design
- This is a randomized, single-blinded study comparing two treatment groups. About 100 participants will be enrolled.
- What's involved
- You will be assigned to one of two pain management groups. Your pain levels and recovery will be tracked daily using a journal and at your first post-operative appointment, which is within one week of surgery.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your pain levels and patient-reported outcomes will be measured for 10 days post-operatively.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Nonopioid Analgesia After Labral Surgery
At a glance
Conditions
NCT03825809
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Henry Ford Health System
Detroit, Michiganno site contact published
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Toufic R Jildeh, MD · PRINCIPAL_INVESTIGATOR · Henry Ford Health System
Who to contact
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Inclusion
What this trial measures
- Pain Levels10 days post-operatively
Patients recorded pain levels 3 times per day using Visual analog scales until study completion. Average daily pain was calculated for each patient. Higher values portend worse control.
- Patient-Reported Outcomes Measurement Information System10 days post-operatively
Patient-Reported Outcomes Measurement Information System Physical Interference (PROMIS PI) nightly until study completion. Average PROMIS PI values calculated nightly. A higher score indicates more pain interference.