Nonopioid Analgesia After Labral Surgery
Recruiting
Phase 2
Phase 3
Interventional Study
Narcotic Use
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Pivotal Trial
This treatment is in the last trial phase before FDA approval.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Trial phase
- Phase 2/3
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 100 (estimated)
- Sponsor
- Henry Ford Health System · Other
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About This Trial
This is a randomized, single blinded, standard of care controlled clinical trial. This project aims to compare postoperative pain control in patients in two treatment arms of rotator cuff repair: a treatment group given a nonopioid pain control regimen, and a standard of care control group given standard opioid pain control regimen
Trial Locations
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Eligibility Criteria
Eligibility Criteria:
Inclusion Criteria:
* All adult patients over age 18 and scheduled for a primary or revision labral surgery
Exclusion Criteria:
* Exclusion criteria will include patients with a medical history of known allergies or intolerance to allergies or intolerance to Celebrex, Tylen…
Contacts