Biceps Tenotomy vs. Tenodesis Impact on Rehabilitation After Rotator Cuff Repair
This observational study aims to compare the impact of Biceps Tenotomy versus Tenodesis on rehabilitation after Rotator Cuff Repair, focusing on assessing your pain level and shoulder function through established scoring systems.
Data Collection
Collected from today forward - ProspectiveCohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: February 1, 2026
Actual date on which the first participant was enrolled.Rotator cuff tears are common in older adults, often causing shoulder instability, pain, and reduced upper limb strength. While non-surgical treatments like physical therapy and medication are usually tried first, surgery may be necessary for some cases. Two common surgical procedures, biceps tenotomy and biceps tenodesis, are often performed alongside rotator cuff repair to alleviate pain and improve function. This study aims to compare the effects of these two procedures on hand grip strength, elbow flexion strength, forearm supination strength, and pain perception in patients undergoing surgical repair for rotator cuff tears. The study's findings could help improve care and address current challenges in treating this condition. During the study, participants will undergo either biceps tenotomy or biceps tenodesis alongside their rotator cuff repair. The study will then measure various outcomes to determine the effectiveness of each procedure. Pain levels will be assessed using a visual analog scale, where patients mark their current pain level on a 100mm line. Shoulder function will be evaluated using two questionnaires: the Arabic version of the American Shoulder and Elbow Surgeons score, and the Constant Score. These questionnaires assess shoulder function, pain, range of motion, and strength. Higher scores on these questionnaires indicate better shoulder function. The study will compare the results between the two surgical procedures to determine which one leads to better outcomes.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.50 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 50 to 70 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Inclusion Criteria: The participant's selection will be based on the following criteria: 1. Both genders adults diagnosed with ≥ 1-cm full-thickness tears of rotator cuff. 2. Age ranged from 50 to 70 years . 3. LHB pathology is involved that will receive ARCR combined with biceps tenotomy or tenodesis. 4. Arthroscopically confirmed LHB pathology. 5. Functionality according to their physical level - Exclusion Criteria: Participants will be excluded if they have any of the following criteria: 1. Massive irreparable tears. 2. Inflammatory arthritis. 3. Thyroid disease. 4. Glenohumeral osteoarthritis. 5. Severe cervical disorders or paralysis of the axillary nerve. 6. Previous surgery of the affected shoulder. 7. Revision surgeries for a rotator cuff tear. 8. Complete LHBT rupture. -
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives