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Impact of Rotator Cuff Repair on Rehabilitation Outcome

Impact of Biceps Tenotomy Versus Tenodesis on Rehabilitation Outcomes After Rotator Cuff Repair

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07394348
Enrollment
50
Registered
2026-02-06
Start date
2026-02-01
Completion date
2027-03-01
Last updated
2026-02-06

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

Conditions

Rotator Cuff Repairs

Keywords

Biceps tenotomy, Biceps tenodesis, Rehabilitation outcomes, Hand grip strength

Brief summary

This study will investigate the difference between BTT (biceps tenotomy ) versus BTD (biceps tenodesis)in patients undergoing rotator cuff repair on postoperative shoulder pain levels, shoulder function, HGS, forearm supination muscle strength, elbow flexion strength

Detailed description

Rotator cuff tears are common musculoskeletal conditions that are often degenerative and typically affect older adults. They may or may not be symptomatic, and their prevalence increases significantly with age, from approximately 9.7% in individuals under 20 years to 62% in those over 80 years. The rotator cuff plays a critical role in stabilizing the shoulder joint through the concavity-compression mechanism, and its dysfunction can result in shoulder instability, pain, and reduced upper limb strength. Conservative management, including physical therapy, therapeutic modalities, and medications, is considered the first-line approach for treating Rotator cuff tears , while surgical intervention is reserved for cases unresponsive to conservative treatment. Among the commonly performed surgical procedures, biceps tenotomy and biceps tenodesis are often combined with rotator cuff repair to alleviate pain and improve functional outcomes. Hand grip strength is widely recognized as a reliable indicator of overall upper limb function and may be affected by both the pathology and its surgical management. Despite its clinical relevance, limited studies have directly compared the impact of Biceps tenotomy and Biceps tenodesis on Hand grip strength. Furthermore, these surgical techniques may influence other functional outcomes, including elbow flexion strength, forearm supination strength, and pain perception. Therefore, this study seeks to investigate and compare the effects of Biceps tenotomy versus Biceps tenodesis on these parameters in patients undergoing surgical repair for rotator cuff tears.

Interventions

DEVICEJamar Handheld dynanometer

is a precision instrument used to measure isometric grip strength. It is widely recognized in clinical research as the "gold standard" for assessing hand strength and general upper-body physical function due to its high test-retest reliability and inter-instrument validity.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to 70 Years
Healthy volunteers
Yes

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. -

Design outcomes

Primary

MeasureTime frameDescription
Pain level3 time intervals ( pre , within 1 week post , 3 months post )Assessed by Visual analog scale : used to assess acute pain particularly effective post-operatively for tracking individual progress . The patients mark their current pain level on a 100 mm horizontal line anchored by verbal descriptors . Scoring is : 0 for No symptoms , 10 for very severe symptoms
shoulder function3 time intervals ( pre , within 1 week post , 3 months post )Will be Assessed by Arabic version of American Shoulder and Elbow Suregeons and Constant Score questionnares \* American shoulder and Elbow Surgeons used to evaluate shoulder function and pain . Patient answer 10 daily activity questions each scored from 0 ( unable) to 3 (normal function ) while the pain assessed by visual analog scale Pain scaore is converted to another 50 point Score total is 100 points ( 50 pain + 50 function ) Higher scores is indication for better shoulder function \* Constant score used to assess shoulder function recovery . It has 2 sections : 1)subjective : 35 points : patient reports on pain and daily activity ability. 2)objective : 65 points : clinical measures for range of motion and strength Grading : pain + activities 0\_35 points Range of motion +strength 0\_65 points Strength is measured as 1 point per pound lifted for 5 sec ..25 points Score total is 100 points .. The higher is better

Secondary

MeasureTime frameDescription
Hand grip strength3 time intervals ( pre , within 1 week post , 3 months post )Will be Assessed by jamar handheld dynanometer Three trials of maximum contraction with holding for 3\_5 seconds will be conducted . The highest value obtained will be used for analysis .
Elbow flexion strength3 time intervals ( pre , within 1 week post , 3 months post )Will be Assessed by jamar handheld dynanometer Three trials of maximum contraction with holding for 3\_5 seconds will be conducted . The highest value obtained will be used for analysis .
Forearm supination strength3 time intervals ( pre , within 1 week post , 3 months post )Will be assessed by jamar handheld dynanometer Three trials of maximum contraction with holding for 3\_5 seconds will be conducted . The highest value obtained will be used for analysis .

Contacts

CONTACTNardin Samuel Nasief
10722023495578@pg.cu.edu.eg01212426966

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026