A comparison between treatments of the biceps tendon during shoulder replacement

Not Applicable

• Conditions: Arthritis of the shoulder; Musculoskeletal - Osteoarthritis; Surgery - Surgical techniques

• Registration Number: ACTRN12612000943842
• Lead Sponsor: Brendan Coleman

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-09-04
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

Patients undergoing anatomic shoulder replacement

Exclusion Criteria

Tumour, fracture, cognitive impairment

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Oxford shoulder score[6 months, 12 months, 2 years]

Secondary Outcome Measures

Name	Time	Method
Constant Shoulder score[6 months, 12 months, 2 years];Disability of Arm, Shoulder, Hand (DASH) score[6 months, 12 months, 2 years]