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NCT04960449 Clinical Trial

Arthroscopic Treatment of Partial Rotator Cuff Tears in Shoulder Joint

Rotator Cuff Tears Clinical Trial

Official title:
Arthroscopic Treatment of Partial-thickness Rotator Cuff Tendon Tears

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04960449
Other study ID # 2014101
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2016
Est. completion date June 2018

Study information
Verified date June 2021
Source Peking University Third Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A retrospective analysis was performed on patients with partial-thickness rotator cuff tendon tears who underwent arthroscopic surgery from August 2006 to December 2011. To evaluate functional outcomes and tendon healing after arthroscopy.

Description:

To study the surgical method and clinical effect of arthroscopic treatment of rotator cuff tendon tear. Retrospective analysis was performed on patients with rotator cuff tendon tears who underwent arthroscopic surgery from August 2006 to December 2011. Preoperative X-ray and MRI were performed. Rotator cuff repair was performed during the operation. UCLA shoulder scoring scale was used to evaluate the shoulder joint at preoperative and final follow-up.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date June 2018
Est. primary completion date June 2017
Accepts healthy volunteers No
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria: - From August 2006 to December 2011, patients with partial-thickness rotator cuff tendon tears who underwent arthroscopic surgery in our department and were successfully followed up. Exclusion Criteria: - Patients with frozen shoulder and shoulder joint instability.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• shoulder arthroscopy
Patients underwent ubacromial bursectomy and acromioplasty , cuff debridement and cuff repair, side to side suture of rotator cuff combined with suture anchor.

Locations
Country Name City State
China Peking University Third Hospital Beijing

Sponsors (1)
Lead Sponsor Collaborator
Peking University Third Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary The function of shoulder joint was analyzed 1 year after arthroscopy. The range of motion and strength of the shoulder joint in all directions are evaluated and recorded. Analysis of UCLA (University of California, Los Angeles) Shoulder Score Scale at 1 year after operation.The UCLA scale has a minimum score of 2 and a maximum score of 35. The higher the score, the better the prognosis of the patients. 1 year after operation
Primary The function of shoulder joint was analyzed 2 years after arthroscopy. The range of motion and strength of the shoulder joint in all directions are evaluated and recorded. Analysis of UCLA Shoulder Score Scale at 2 years after operation 2 years after operation
Primary The function of shoulder joint was analyzed 5 years after arthroscopy. The range of motion and strength of the shoulder joint in all directions are evaluated and recorded. Analysis of UCLA Shoulder Score Scale at 5 years after operation 5 years after operation
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