NCT06774820

Brief Summary

The aim of this study is to compare the clinical results and complications of self-locking biceps tenodesis and double 360 lasso loop biceps tenodesis for the treatment of long chief of biceps or superior labrum anterior-posterior (SLAP) tendon pathology during shoulder arthroscopy in patients undergoing arthroscopic rotator cuff repair. Currently, there is no consensus on the use of tenodesis versus tenotomy to treat pathology of the long head of the biceps during arthroscopic rotator cuff repair. Numerous studies have examined the clinical results of long biceps tenotomy versus long biceps tenodesis, and there is no evidence to date of superiority of either technique. At Clinique Générale, we use a new, innovative technique called autobloc tenodesis to treat pathologies of the long head of the biceps. There are no comparative studies between autobloc tenodesis of the biceps and biceps tenodesis. Given its potential advantages, self-locking biceps tenodesis could emerge as the new technique of choice for treating biceps longus tendon pathology, potentially reducing differences in outcomes such as Popeye deformity. The information provided by this study could potentially guide future clinical practice, helping surgeons to choose the most appropriate treatment for their patients suffering from long biceps tendon pathology.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
20mo left

Started Jan 2025

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress43%
Jan 2025Jan 2028

First Submitted

Initial submission to the registry

January 9, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

January 14, 2025

Completed
8 days until next milestone

Study Start

First participant enrolled

January 22, 2025

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 15, 2027

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 15, 2028

Last Updated

February 12, 2025

Status Verified

February 1, 2025

Enrollment Period

2.8 years

First QC Date

January 9, 2025

Last Update Submit

February 11, 2025

Conditions

Keywords

rotator cuffbicepslong biceps tendon

Outcome Measures

Primary Outcomes (1)

  • Constant score (CMS)

    The CMS is a 100-point scale comprising four components, including a patient-reported section (pain 15 points and activity level 20 points), for a total of 35 points. Alongside this, there is a doctor-reported section (shoulder strength 25 points, range of motion 40 points) for a total of 65 points.

    1 year after surgery

Secondary Outcomes (1)

  • American Shoulder and Elbow Surgeons Score

    3 months, 6 months, 1 year after surgery

Study Arms (2)

self-blocking tenodesis

EXPERIMENTAL
Procedure: self-blocking tenodesis

arthroscopic tenodesis

ACTIVE COMPARATOR
Procedure: arthroscopic tenodesis

Interventions

the LHB tendon is detached from its origin in the superior labrum. This technique supports the self-locking mechanism of the LHB tendon in the bicipital groove by detaching the tendon from the Y-shaped superior glenoid, including the superior labrum. A radiographically visible suture will be attached to the proximal part of the LHB tendon to facilitate later localization of the LHB tendon during imaging (3-0 stainless steel, ethicon).

self-blocking tenodesis

LHB tendon is detached from its origin, and sutured. Next, the LHB tendon is fixed in the bicipital groove using a 360-lasso loop tenodesis technique. A radiographically visible suture will be attached to the proximal part of the LHB tendon to facilitate subsequent localization of the LHB tendon during imaging (3-0 stainless steel, ethicon).

arthroscopic tenodesis

Eligibility Criteria

Age40 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Full-thickness rotator cuff tear of the supraspinatus/infraspinatus tendon, diagnosed preoperatively by ultrasound, arthro-CT or MRI.
  • Patients must be able to read and write in French in order to complete the questionnaires and sign the informed consent form.

You may not qualify if:

  • Partial rotator cuff tear
  • Massive and irreparable rotator cuff tear
  • Grade 4 according to Goutallier classification of fatty degeneration of rotator cuff muscles
  • Rupture of the long biceps
  • Hourglass deformity of biceps tendon origin
  • Osteoarthritis of the glenohumeral joint, defined by narrowing of the glenohumeral joint space or osteophytes, using AP radiography of the affected shoulder.
  • Distance between acromion and humeral head measuring 6 mm or less, defined by Hamada classification as grade 2 or higher.
  • Previous shoulder surgery.
  • Dementia or inability to complete questionnaires and assessments.
  • Pregnant, parturient or breast-feeding patients.
  • Persons under legal protection (curatorship, guardianship, safeguard of justice).
  • Persons deprived of their liberty by judicial or administrative measure
  • Persons under psychiatric care
  • Persons not affiliated to a social security scheme

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Clinique Générale

Annecy, 74000, France

RECRUITING

Related Publications (1)

  • Shirinskiy IJ, Boulidam D, Macken AA, van den Bekerom MPJ, Lafosse T, Buijze GA. Biceps lasso loop and self-locking tenodesis alongside repair of rotator cuff tears: randomised controlled trial study protocol (BLAST 1). BMJ Open. 2025 Nov 19;15(11):e106475. doi: 10.1136/bmjopen-2025-106475.

MeSH Terms

Conditions

Rotator Cuff Injuries

Condition Hierarchy (Ancestors)

RuptureWounds and InjuriesShoulder InjuriesTendon Injuries

Central Study Contacts

Geert Alexander Buijze, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 9, 2025

First Posted

January 14, 2025

Study Start

January 22, 2025

Primary Completion (Estimated)

November 15, 2027

Study Completion (Estimated)

January 15, 2028

Last Updated

February 12, 2025

Record last verified: 2025-02

Data Sharing

IPD Sharing
Will not share

Locations