Adhesion prophylaxis for shoulder prosthesis operations

Not Applicable

Recruiting

• Conditions: M75.0; Adhesive capsulitis of shoulder

• Registration Number: DRKS00033913
• Lead Sponsor: Paracelsus Klinik Bremen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-04-08
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Inverse and anatomical shoulder TEPs, written consent

Exclusion Criteria

Coagulation disorders, previous surgery on the corresponding shoulder, post-traumatic conditions on the corresponding shoulder, socket-free inverse prostheses, rehab without CPM chair

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Relative Constant-Murley Score after 12 weeks (calculated as the difference to the preoperative value)

Secondary Outcome Measures

Name	Time	Method
- Constant-Murley Score after 4 weeks and 1 year<br> - Subcategories of the Constant-Murley Score (pain, everyday life, motility (active), strength) analyzed individually (after 4, 12 weeks, and 1 year)<br> - Passive motility, determined equivalent to active motility as described in the Constant-Murley Score (after 4 and 12 weeks and 1 year)<br> - ASES questionnaire (after 4 and 12 weeks and 1 year) including a separate comparison of subcategory results<br> - Hb/Hk values on post-op days 1 and 4 <br>- Drainage volume on the first postoperative day<br> - Drainage duration