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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05660031
Other study ID # 2021-00066
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 1, 2021
Est. completion date June 1, 2025

Study information

Verified date March 2024
Source La Tour Hospital
Contact Alexandre Lädermann, MD
Phone +41 22 71 975 55
Email alexandre.laedermann@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The long head of the biceps (LHB) tendon is thought to be a common source of shoulder pain and dysfunction in patients with rotator cuff pathology. Tenotomy and tenodesis have been shown to produce favourable and comparable results in treating LHB lesions, but a controversy still exists regarding the treatment of choice. Some suggest that tenotomy should be reserved for older, low-demand patients, while tenodesis should be performed in younger patients and those who engage in heavy labor. Proponents of tenotomy suggest that this is a technically easy procedure that leads to easy rehabilitation and fast return to activity with a low complication and reoperation rate. However, those who support LHB tenodesis list good preservation of elbow flexion and supination strength, improvement of functional scores, elimination of pain, and avoidance of cosmetic deformity as benefits of the procedure. Alternatively, the LHB can be maintained in the joint without tenodesis or tenotomy. In fact, it has not been clearly shown that LHB tenodesis or tenotomy leads to improved outcomes compared to leaving the biceps tendon intact.


Description:

The long head of the biceps (LHB) tendon is thought to be a common source of shoulder pain and dysfunction in patients with rotator cuff pathology.Tenotomy and tenodesis have been shown to produce favourable and comparable results in treating LHB lesions, but a controversy still exists regarding the treatment of choice. Some suggest that tenotomy should be reserved for older, low-demand patients, while tenodesis should be performed in younger patients and those who engage in heavy labor. Proponents of tenotomy suggest that this is a technically easy procedure that leads to easy rehabilitation and fast return to activity with a low complication and reoperation rate. However, those who support LHB tenodesis list good preservation of elbow flexion and supination strength, improvement of functional scores, elimination of pain, and avoidance of cosmetic deformity as benefits of the procedure. Alternatively, the LHB can be maintained in the joint without tenodesis or tenotomy. In fact, it has not been clearly shown that LHB tenodesis or tenotomy leads to improved outcomes compared to leaving the biceps tendon intact. The primary goal of this prospective multicenter randomized study is to evaluate whether LHB tenodesis grants superior post-operative functional outcomes compared to LHB tenotomy or leaving the LHB intact in patients undergoing rotator cuff repair (RCR) for an isolated full-thickness lesion of the supraspinatus. The primary goal of this prospective multicenter randomized study is to evaluate whether LHB tenodesis grants superior post-operative functional outcomes compared to LHB tenotomy or leaving the LHB intact in patients undergoing rotator cuff repair (RCR) for an isolated full-thickness lesion of the supraspinatus. The secondary goals are to determine whether there is a difference in post-operative functional outcomes between the LHB tenotomy group and the Intact LHB group, and if there is a difference in complication rates or patient satisfaction between the three groups.


Recruitment information / eligibility

Status Recruiting
Enrollment 180
Est. completion date June 1, 2025
Est. primary completion date June 1, 2025
Accepts healthy volunteers No
Gender All
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria: - Patient voluntarily consents to participate in the study and has the mental and physical ability to participate in the study, fill out subjective questionnaires, return for follow-up visits, and comply with prescribed post-operative physical therapy. - Full thickness tear of the supraspinatus tendon - Intact subscapularis tendon - Primary rotator cuff repair - Age 50-80 Exclusion Criteria: - Previous full thickness biceps tear - Infection and neuropathic joints - Known or suspected non-compliance, drug or alcohol abuse - Patients incapable of judgement or under tutelage - Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, contraindication for MRI scan etc. - Enrolment of the investigator, his/her family members, employees and other dependent persons - Patient declines to participate in study

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
LHB Tenotomy
Will be performed arthroscopically by cutting the LHB at its origin with arthroscopic scissors
LHB Tenodesis
"ill be performed arthroscopically with a tenodesis at the top of the articular margin using an onlay technique.

Locations

Country Name City State
Canada Group 23 Sports Medicine Calgary Alberta
Switzerland la Tour hospital Meyrin Geneva
United States Sports Medicine and Shoulder Surgery, University of Michigan Ann Arbor Michigan
United States Oregon Health & Science University Portland Oregon

Sponsors (1)

Lead Sponsor Collaborator
La Tour Hospital

Countries where clinical trial is conducted

United States,  Canada,  Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary ASES score American Shoulder and Elbow Surgeon (ASES) score. From 0 (worst) to 100 (best). At 24 post-operative months
Secondary VAS pain Visual analog scale (VAS) pain. From 0 (best) to 10 (worst) At 24 post-operative months
Secondary SSV Subjective Shoulder Value (SSV). From 0 (worst) to 100 (best). At 24 post-operative months
Secondary LHB score Long head of the biceps (LHB) score. From 0 (worst) to 100 (best). At 24 post-operative months
Secondary AFF Anterior Forward Flexion. In degrees. Will be performed with a goniometer by an independent investigator At 24 post-operative months
Secondary ER at side External Rotation at the side. In degrees. Will be performed with a goniometer by an independent investigator At 24 post-operative months
Secondary IR Internal Rotation to nearest spinal level. Will be performed with a goniometer by an independent investigator At 24 post-operative months
Secondary Complications Any type of post-operative complication Within 2 postoperative years
Secondary Patient satisfaction Yes or no At 24 post-operative months
Secondary Location of the defect (at the foot print | medial cuff failure) Radiographic outcome evaluated using an ultrasound examination. At 6 post-operative month
Secondary Status of the biceps tendon (intact | in continuity | defect) Radiographic outcome evaluated using an ultrasound examination. At 6 post-operative month
Secondary Signs of anchor displacement and location (lateral | medial row). Radiographic outcome evaluated using an ultrasound examination. At 6 post-operative month
Secondary Tendon thickness Radiographic outcome evaluated using an ultrasound examination. At 6 post-operative month
Secondary Number of patients with bursitis Radiographic outcome evaluated using an ultrasound examination. At 6 post-operative month
Secondary Number of patients with healing of the Supraspinatus tear according to Sugaya classification Radiographic outcome evaluated using an ultrasound examination. At 6 post-operative month
Secondary Number of patients with liquid in the bicipital sheath Radiographic outcome evaluated using an ultrasound examination. At 6 post-operative month
Secondary Number of patients with hypervascularization of the sheath Radiographic outcome evaluated using an ultrasound examination. At 6 post-operative month
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