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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05823428
Enrollment
40
Registered
2023-04-21
Start date
2019-02-01
Completion date
2022-01-01
Last updated
2023-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Partial Thickness Rotator Cuff Tears

Keywords

partial thickness, bursal side, rotator cuff, full thickness, subacromial bursa

Brief summary

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

Interventions

PROCEDUREAugmentation with subacromial bursa + acromioplasty

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

PROCEDURERotator cuff debridement + acromioplasty

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

Sponsors

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of biological augmentation with bursa using postoperative clinical scores and MRI.18 monthsOur 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026