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Rotator Cuff Tears Treated With Long Head of the Biceps Reinforcement

Evaluation of Rotator Cuff Repair With Long Head of the Biceps Reinforcement: a Prospective Randomized Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06664645
Enrollment
60
Registered
2024-10-29
Start date
2022-01-14
Completion date
2025-04-14
Last updated
2025-06-26

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

Conditions

Biceps Tendon Reattachment, Rotator Cuff Injuries

Keywords

rotator cuff, tendon transfer, biceps reinforcement, biceps autograft

Brief summary

The increase of the population life expectancy and the active lifestyle adopted in recent years have contributed to the higher incidence of rotator cuff injuries. For large (\>3 cm) and extensive (\>5 cm) injuries of the rotator cuff, even after complete or partial repair, the chances of failure reach 94%. An alternative in rotator cuff injuries is the use of the long head of the biceps (LHB) as an autologous graft to increase the healing rate and the final outcomes. The primary objective is to compare the functional results, according to the ASES score, between patients who use or not the long head biceps brace for complete repairs of large and extensive rotator cuff tears. The secondary objectives are to compare the groups according to structural results by MRI and functional results by the UCLA score.

Detailed description

A prospective randomized study will be carried out in a 1:1 ratio between groups. Patients with large and extensive rotator cuff injuries will be selected at the Shoulder and Elbow clinic of Pedro Ernesto University Hospital (HUPE-UERJ), during outpatient care. Patients with an intact long head of the biceps will be randomized into two groups, according to the use or not of the tendon: complete repair with LHB tendon reinforcement and complete repair without reinforcement. All patients will be operated by the same surgeon. All selected patients will be explained what the research is about by a research assistant not involved in the treatment and will be offered the option to participate or not. The American Shoulder and Elbow Surgeons Standardized Shoulder Assessment Form (ASES) scale will be adopted as the primary outcome. The Modified University of California at Los Angeles Shoulder Rating Scale (UCLA) and the assessment of tendon healing with magnetic resonance imaging at 6 months after surgery, using the classification of Sugaya et al. will be secondary outcomes.

Interventions

PROCEDURELHB tendon reinforcement

complete repair with LHB tendon reinforcement

PROCEDUREcomplete repair without reinforcement

conventional rotator cuff complete repair without reinforcement

Sponsors

Hospital Universitario Pedro Ernesto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

A prospective randomized study will be carried out in a 1:1 ratio between groups. Patients with large and extensive rotator cuff injuries will be selected at the Shoulder and Elbow clinic of Pedro Ernesto University Hospital (HUPE-UERJ), during outpatient care. Patients with an intact long head of the biceps will be randomized into two groups, according to the use or not of the tendon: complete repair with LHB tendon reinforcement and complete repair without reinforcement.

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Long head tendon of biceps intact; * Large or extensive posterosuperior rotator cuff injuries according to the classification of DeOrio and Cofield;20 * Fatty degeneration of the ≦2 supraspinatus muscle according to the classification of Goutallier.21

Exclusion criteria

* Active or previous infection in the affected shoulder; * Patients unable to understand preoperative questionnaires; * Patient who does not undergo at least 1 postoperative evaluation. * Injury where complete repair of the rotator cuff is not possible; * Rupture of the LHB tendon diagnosed intraoperatively.

Design outcomes

Primary

MeasureTime frameDescription
Visual analogue score (VAS)24 monthsVisual analogue score: it is a 10 cm line with two end points, one representing no pain and the other representing worst pain. The patient marks the line to indicate their current pain level, and the distance from the no pain marker to the mark is measured in centimeters to provide a score. A higher score indicates greater pain intensity.
Structural outcomes24 monthsPatients will undergo preoperative MRI and from 6 months after the procedure. All images will be evaluated by at least two authors of the work, who will not know which group the patients belong to. The classification by Sugaya et al. stratifies the appearance of the tendon after repair into 5 types: type I (sufficient thickness with low signal in all images); type II (sufficiently thick with high focal signal); type III (insufficient thickness without discontinuity); type IV (small size tear) and type V (medium or large size tear). The healing of the long head biceps reinforcement will also be evaluated by MRI and classified as unhealed and healed.
American Shoulder and Elbow Score (ASES)24American Shoulder and Elbow Score score ranges from 0 to 100, with 0 the lowest level of function and 100 the highest level of function.
The University of California-Los Angeles (UCLA)24 monthsScores ranged from 0 to 35 with a score of 0 indicating worst shoulder function and 35 indicating best shoulder function.
The 12 item Short Form Survey (SF-12)24 monthsThis is a self-reported outcome measure assessing the impact of health on an individual's everyday life. It is often used as a quality of life measure. Utilize the norm-based scoring system to interpret Physical component and Mental component scores, with a mean of 50 and a standard deviation of 10 in the general population. Scores above 50 indicate a better-than-average health-related quality of life, while scores below 50 suggest below-average health.

Countries

Brazil

Outcome results

None listed

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