Results of Arthroscopic Massive Rotator Cuff Tears Repair With or Without Using Long Head of Biceps Tendon
- Conditions
- Rotator Cuff Tears
- Registration Number
- NCT05817071
- Lead Sponsor
- Ain Shams University
- Brief Summary
The Goal of this clinical trial is to asses the function of arthroscopic repair with or without superior capsular augmentation using biceps tendon .
- Detailed Description
All patients included in this clinical trial Will be informed by written consent will undergo a one week screening to determine the eligibility for study entry. Patients who meet the eligibility requirements Will be randomised in a single blinded manner ( patients).
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 30
- age 40 to 80 years old
- Patients with massive rotator cuff tear
- patients with glenohumeral arthritis
- Acromioclavicular arthritis that requires distal clavicle resection
- Patients with other intra articular pathology like slap lesion
- Neural damage( brachial plexus injury)
- Revision cases
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Functional shoulder constant score (assess the change pre operative and post operative during study period completion) 1- preoperative 2- six months post operative 3- one year post operative Assess the change of Constant score of the patients pre operative and during follow up duration of the study on multiple periods (a multi-item functional scale assessing pain, activity of daily living , range of motion and strength of the affected shoulder. Its score ranges from 0 to 100 points, representing worst and best shoulder function, respectively.)
Functional shoulder ases score (assess the change preoperative and postoperative during study period completion ) 1- preoperative 2- six months post operative 3- one year post operative Assess the change in Ases score pre operative and post operative during study completion on multiple periods ( American shoulder and elbow surgeons standardized form)Scores range from 0 to 100 with a score of 0 indicating a worse shoulder condition and 100 indicating a better shoulder condition.
- Secondary Outcome Measures
Name Time Method Shoulder Pain ( assess the change preoperative and postoperative during the study period completion) 1 pre operative 2 two weeks post operative 3 six months post operative Asses the change in the visual analog score ( zero equal no pain and 10 equal severest pain ) pre operative and post operative during study period on different periods
Trial Locations
- Locations (1)
Mostafa Ahmed Mohamed Mostafa,MSC
🇪🇬Cairo, Abbasia, Egypt
Mostafa Ahmed Mohamed Mostafa,MSC🇪🇬Cairo, Abbasia, Egypt