Status:
RECRUITING
Nonopioid Analgesia After Labral Surgery
Lead Sponsor:
Henry Ford Health System
Conditions:
Narcotic Use
Eligibility:
All Genders
18+ years
Phase:
PHASE2
PHASE3
Brief Summary
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 tr...
Detailed Description
Study Design: This is a randomized, single blinded, standard of care-controlled clinical trial. All adult patients over eighteen desiring rotator cuff repair will be eligible. Nonnarcotic postoperativ...
Eligibility Criteria
Inclusion
- Eligibility Criteria:
- All adult patients over age 18 and scheduled for a primary or revision labral surgery
Exclusion
- Exclusion criteria will include patients with a medical history of known allergies or intolerance to allergies or intolerance to Celebrex, Tylenol, Neurontin, dexamethasone, tramadol, substantial alcohol or drug abuse, and pregnancy, history of narcotics within 6 months of surgery, renal impairment, peptic ulcer disease, GI bleeding. Secondary exclusion criterion is an intact rotator cuff
Key Trial Info
Start Date :
January 22 2019
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 20 2020
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT03825809
Start Date
January 22 2019
End Date
May 20 2020
Last Update
January 31 2019
Active Locations (1)
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1
Henry Ford Health System
Detroit, Michigan, United States, 48202