ACTRN12606000195550
Completed
Not Applicable
A study of the efficacy of the addition of a ropivacaine infusion to the analgesia provided by pre-emptive ropivacaine and intra-operative parecoxib for reduction of peri-operative pain in adults undergoing elective arthroscopic rotator cuff surgery: a randomised double blind placebo controlled trial.
Monash University, Jennifer Coghlan PhD Scholar, Supervisors, A/Prof. Rachelle Buchbinder and A/Prof. Andrew Forbes.0 sites158 target enrollmentMay 24, 2006
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Rotator cuff surgery
- Sponsor
- Monash University, Jennifer Coghlan PhD Scholar, Supervisors, A/Prof. Rachelle Buchbinder and A/Prof. Andrew Forbes.
- Enrollment
- 158
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Requiring rotator cuff surgery either subacromial decompression or tendon repair.
Exclusion Criteria
- •Previous surgery to that shoulderFractures or tumoursIrreparable tendon tears.
Outcomes
Primary Outcomes
Not specified
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