ACTRN12607000150448RecruitingNot Applicable
A prospective randomised control trial comparing post-operative pain relief after shoulder surgery, using regional anaesthesia inter-scalene block, compared with direct shoulder joint anaesthesia using a breg pump following arthroscopic rotator cuff repair of the shoulder for those patients with rotator cuff arthropathy
igel Hartnett0 sites50 target enrollmentStarted: March 1, 2007Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 50
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Randomised controlled trial
- Primary Purpose
- Treatment
- Masking
- Open (masking not used)
Eligibility Criteria
- Ages
- 16 Years to ot stated (—)
- Sex
- All
Inclusion Criteria
- •1. All patients with a rotator cuff tear / arthropathy at Mercy Hospital who will2. undergo arthroscopic rotator cuff repair by Simon McMahon 3. be anaesthetised by John Hyndman4. All patients who wish to participate in the study and give consent to being in the study.
Exclusion Criteria
- •Those patients not able to give consent. Those patients who are sensitive or allergic to the medications given. Those patients who do not wish to participate and/or who do not give consent to being in the study.
Investigators
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