Opioid-Free Study in Arthroscopic Rotator Cuff Repair

Rothman Institute Orthopaedics

Status: Completed

Conditions: Rotator Cuff Tears

Study type: Observational

Funder types: Other

Identifiers

NCT04277208

2018LAustin

Details and patient eligibility

About

The purpose of this study is to develop and test an opioid-free pain control protocol for patients undergoing arthroscopic rotator cuff repair.

Enrollment: 36 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• All patients over the age of 18
• clinically indicated for an Arthroscopic Rotator Cuff Repair (ARCR)

Exclusion criteria

• Patients with irreparable rotator cuff tears
• allergic or sensitivity to the study medication
• intolerance to pain protocol
• history of gastrointestinal issues
• renal disease
• any evidence of glenohumeral arthritis

Trial design

36 participants in 1 patient group

Arthroscopic Rotator Cuff Repair