Arthroscopic Treatment of Bursal-side Rotator Cuff Tears in Shoulder Joint

Arthroscopic Treatment of Bursal-side Partial-thickness Rotator Cuff Tears

A retrospective analysis was performed on patients with bursal-side partial-thickness rotator cuff tears who underwent arthroscopic surgery from January 2009 to December 2011. To investigate the diagnosis and arthroscopic treatment of partial rotator cuff bursa lateral tear, and to evaluate the postoperative functional outcome and tendon healing.

Study Overview

• Status: Completed
• Conditions: Rotator Cuff Tears
• Intervention / Treatment: Procedure: shoulder arthroscopy

Detailed Description

To study the surgical method and clinical effect of arthroscopic treatment for partial tear of rotator cuff bursa. A retrospective analysis was performed on patients bursal-side partial-thickness rotator cuff tears who underwent arthroscopic surgery from January 2009 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 joint at preoperative and final follow-up.

• Study Type: Observational
• Enrollment (Actual): 50

Contacts and Locations

Study Locations

• China
  • Beijing, China, 100083
    • Peking University Third Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 20 years to 70 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

Patients diagnosed with bursal-side partial-thickness rotator cuff tears, there has been very little research on bursal-side partial-thickness rotator cuff tears, which has no consensus on diagnosis and treatment.

Description

Inclusion Criteria:

• From January 2009 to December 2011, patients with bursal-side partial-thickness rotator cuff tears who underwent arthroscopic surgery at Peking University Third Hospital and were followed up.

exclude:

Exclusion Criteria:

• Patients with frozen shoulder and unstable shoulder joints.

Study Plan

How is the study designed?

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
patients with bursal-side partial-thickness rotator cuff tears; Patients with bursal-side partial-thickness rotator cuff tears who underwent arthroscopic surgery and was followed up at Peking University Third Hospital.	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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
UCLA (University of California, Los Angeles) Shoulder Score Scale at 1 year after operation.	Analysis of UCLA (University of California, Los Angeles) Shoulder Score Scale at 1 year after operation. The 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
UCLA (University of California, Los Angeles) Shoulder Score Scale at 2 years after operation.	Analysis of UCLA (University of California, Los Angeles) Shoulder Score Scale at 2 years after operation.The scale has a minimum score of 2 and a maximum score of 35. The higher the score, the better the prognosis of the patients.	2 years after operation
UCLA (University of California, Los Angeles) Shoulder Score Scale at 5 years after operation.	Analysis of UCLA (University of California, Los Angeles)Shoulder Score Scale at 5 years after operation. The scale has a minimum score of 2 and a maximum score of 35. The higher the score, the better the prognosis of the patients.	5 years after operation

Collaborators and Investigators

• Sponsor: Peking University Third Hospital
• Investigators: Principal Investigator: jian xiao, Peking University Third Hospital

Study record dates

Study Major Dates

• Study Start (Actual): June 1, 2016
• Primary Completion (Actual): June 1, 2016
• Study Completion (Actual): June 1, 2017

Study Registration Dates

• First Submitted: June 27, 2021
• First Submitted That Met QC Criteria: July 29, 2021
• First Posted (Actual): August 2, 2021

Study Record Updates

• Last Update Posted (Actual): August 2, 2021
• Last Update Submitted That Met QC Criteria: July 29, 2021
• Last Verified: June 1, 2021

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Wounds and Injuries; Rupture; Shoulder Injuries; Tendon Injuries; Rotator Cuff Injuries
• Other Study ID Numbers: 2014100

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No