Arthroscopic Biological Augmentation With Subacromial Bursa for Bursal Side Partial-thickness Rotator Cuff Tears

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization40 enrolled

Overview

The investigators aimed to compare the results of acromioplasty + arthroscopic debridement and acromioplasty + augmentation with subacromial bursa.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Partial Thickness Rotator Cuff Tears

Interventions

Augmentation with subacromial bursa + acromioplastyPROCEDURE

Two intervention was planned. Rotator cuff debridement + acromioplasty group is mentioned as Group A (18 patients) and augmentation with subacromial bursa + acromioplasty is Group B

Rotator cuff debridement + acromioplastyPROCEDURE

Two intervention was planned. Rotator cuff debridement + acromioplasty group is mentioned as Group A (18 patients) and augmentation with subacromial bursa + acromioplasty is Group B

Eligibility

Sex: ALLMin age: 25 YearsMax age: 65 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * bursal side rotator cuff tears in MRI sections * Patients whose pain does not go away despite NSAIDs and standardized physical therapy by the same physiotherapist applied for 3 months * 25-50% or 3-6 mm rotator cuff tear (Ellman grade 2) on the bursal side Exclusion Criteria: * Previous surgery * tears greater than 50% or 6 mm

Locations (1)

SBU Prof. Cemil Tascioglu City Hospital

Istanbul, Turkey (Türkiye)

Outcomes

Primary Outcomes

Evaluation of biological augmentation with bursa using postoperative clinical scores and MRI.

Our Primary Outcome Measure is to investigate the effects of biological augmentation with subacromial bursa in arthroscopic bursal-sided partial thickness rotator cuff repair with postoperative MRI and functional scores with Constant-Murley and Ases scores.

Time frame: 18 months

Data from ClinicalTrials.gov

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