NCT06774820 Biceps Lasso Loop and Self- Locking Tenodesis Alongside Repair of Rotator Cuff Tears: Randomised Controlled Trial Study Protocol (BLAST 1)
| NCT ID | NCT06774820 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Clinique Générale dAnnecy |
| Condition | Rotator Cuff Injury |
| Study Type | INTERVENTIONAL |
| Enrollment | 100 participants |
| Start Date | 2025-01-22 |
| Primary Completion | 2027-11-15 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 100 participants in total. It began in 2025-01-22 with a primary completion date of 2027-11-15.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
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.
Eligibility Criteria
Inclusion Criteria: * Rotator cuff tear: confirmed preoperative diagnosis of a non- traumatic, full- thickness tear of the supraspinatus and/or infraspinatus and/or subscapularis tendon, as evidenced by ultrasound, arthro- CT or MRI. * Language proficiency: sufficient to allow for communication during the informed consent process and for the completion of the study questionnaires. Exclusion Criteria: * Tear type: partial thickness rotator cuff tears are excluded. * Tear severity: individuals with massive or irreparable rotator cuff tears are excluded. * Fatty degeneration: presence of rotator cuff muscle fatty degeneration classified as Grade 4 according to the Goutallier system will result in exclusion. * Glenohumeral osteoarthritis: patients exhibiting glenohumeral osteoarthritis, defined radiographically by the presence of joint space narrowing or osteophytes on anteroposterior (radiographs of the affected shoulder) will be excluded. * Prior shoulder surgery: history of previous surgical intervention on the affected shoulder will result in exclusion. * Popeye sign: preoperative presence of the Popeye sign will result in exclusion. * Cognitive impairment: pre- existing dementia or any condition that impairs the ability to understand study procedures and complete questionnaires and assessments is an exclusion criterion. * 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 & Investigator
Frequently Asked Questions
Who can join the NCT06774820 clinical trial?
This trial is open to participants of all sexes, aged 40 Years or older, studying Rotator Cuff Injury. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06774820 currently recruiting?
Yes, NCT06774820 is actively recruiting participants. Contact the research team at gabuijze@hotmail.com for enrollment information.
Where is the NCT06774820 trial being conducted?
This trial is being conducted at Annecy, France.
Who is sponsoring the NCT06774820 clinical trial?
NCT06774820 is sponsored by Clinique Générale dAnnecy. The trial plans to enroll 100 participants.