Traditional vs. Nonopioid Analgesia After Labral Surgery
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2/Phase 3
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 treatment group given a nonopioid pain control regimen, and a standard of care control group given standard opioid pain control regimen
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:
• All adult patients over age 18 and scheduled for a primary or revision labral surgery
Locations
United States
Michigan
Henry Ford Health System
RECRUITING
Detroit
Contact Information
Primary
Toufic R Jildeh, MD
tjildeh1@hfhs.org
517-230-8511
Time Frame
Start Date: 2019-01-22
Estimated Completion Date: 2020-05-20
Participants
Target number of participants: 100
Treatments
Experimental: Post-Operative Non Opioid Pain Protocol
Patients will be administered a post-operative non-opioid pain protocol consisting of:~Celecoxib Ketorolac Gabapentin Acetaminophen Diazepam
Active_comparator: Post-Operative Traditional Pain Protocol
Patients will be administered a traditional post-operative pain protocol consisting of: Hydrocodone-acetaminophen 5-325
Related Therapeutic Areas
Sponsors
Leads: Henry Ford Health System