Post-operative pain management following arthroscopic rotator cuff repair. A comparison of inter-scalene block with subacromial bursal infusio

Recruiting

• Conditions: Rotator cuff tear / arthropathy; Anaesthesiology - Other anaesthesiology; Musculoskeletal - Other muscular and skeletal disorders

• Registration Number: ACTRN12607000150448
• Lead Sponsor: igel Hartnett

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2007-03-01
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 50

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.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
evel of Pain following surgery[Pre-operation, 4, 8, 12, 24, and 48 hours post-operation];Visual analogue scale[Pre-operation, 4, 8, 12, 24, and 48 hours post-operation]

Secondary Outcome Measures

Name	Time	Method
Other medications used[Pre-operation, 4, 8 ,12, 24 and 48 hours post-operation.]