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Study identifier: NCT07375277 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effects Of Biceps Transposition Without Tenotomy For Augmentation Of Massive Rotator Cuff Repairs

Condition: Massive Rotator Cuff Tear  ·  Sponsor: Ataturk University

PhaseNA
Planned participants35
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This prospective, single-arm interventional study will evaluate the effects of long head of the biceps tendon (LHBT) transposition without tenotomy as an augmentation technique for arthroscopic partial repair in adults with massive rotator cuff tears. Consecutive eligible patients undergoing arthroscopic partial rotator cuff repair plus tenotomy-sparing LHBT transposition augmentation at Balikesir City Hospital (Balikesir, Turkiye) will be enrolled and followed for 12 months. Patient-reported outcomes and clinical assessments will be collected preoperatively (baseline) and postoperatively at 3 and 12 months. The primary outcomes are shoulder function (ASES), rotator cuff-related quality of life (WORC converted to a 0-100 scale), and sleep disturbance (Insomnia Severity Index). Secondary outcomes include active shoulder range of motion and biceps-related clinical findings (Speed test, Yergason test, bicipital groove tenderness, and Popeye deformity). Postoperative MRI will not be obtained routinely and will be performed only if clinically indicated. The study aims to provide standardized prospective data on functional outcomes, quality of life, and sleep after this augmentation approach.

This description comes directly from the study's public registry record.

Talk to the study team

gunes 0 SARIKAYA, M.D  ·  05436733113  ·  gunessarikaya05@hotmail.com

gunes SARIKAYA  ·  05436733113

Always discuss trial participation with your own doctor first.

Locations (1)

Güneş SarıkayaBalıkesir, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07375277