Arthroscopic Rotator Cuff Repair With Multimodal Analgesia(MMA)

Not Applicable

Completed

• Conditions: Rotator Cuff Tear
• Interventions: Procedure: Arthroscopic rotator cuff repair with intraoperative periarticular injection; Procedure: Arthroscopic rotator cuff repair with non-injection of MMA drugs

• Registration Number: NCT01204606
• Lead Sponsor: Seoul National University Hospital

Brief Summary

* The purpose of this study is to compare the efficacy of periarticular injections consisting of ropivacaine, morphine, epinephrine, cefotetan, and hyaluronic acid with the efficacy of periarticular injections consisting of the same amount of placebo(isotonic saline) during arthroscopic rotator cuff repair.

* Adding of multimodal analgesia(MMA) to conventional rotator cuff repair, it was expected that could reduce postoperative pain and narcotic consumption.

Detailed Description

Not available

Study Timeline

• Study Start: 2010-09
• Study First Submitted: 2010-09-16
• Study First Submitted QC: 2010-09-16
• Study First Posted: 2010-09-17
• Primary Completion: 2011-03
• Status Verified: 2013-03
• Last Update Submitted: 2013-03-11
• Last Update Posted: 2013-03-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 54

Inclusion Criteria

• rotator cuff tear
• arthroscopic surgery

Exclusion Criteria

• age<45 or >85
• allergies to the drugs used in the study
• acute trauma history
• history of renal disease
• history of hepatic disease
• osteoarthritis or rheumatic arthritis
• systemic condition with chronic pain
• history of infection
• could not understand the questions
• rotator cuff tear treated by the open technique, by debridement only

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
MMA group	Arthroscopic rotator cuff repair with intraoperative periarticular injection	-
Control group	Arthroscopic rotator cuff repair with non-injection of MMA drugs	-

Primary Outcome Measures

Name	Time	Method
Visual Analogue Scale(VAS) for Pain	postoperative 5 hours

Secondary Outcome Measures

Name	Time	Method
Postoperative narcotic consumption	every 6 hours after surgery

Trial Locations

Locations (1)

Joint and Spine Center; SMG-SNU Boramae Medical Center; 🇰🇷 Seoul, Korea, Republic of