Skip to content

Clinical Outcomes After Arthroscopic Tenotomy or Tenodesis of the Long Head of the Biceps

Clinical Outcomes After Arthroscopic Tenotomy or Tenodesis of the Long Head of the Biceps

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02811757
Enrollment
100
Registered
2016-06-23
Start date
2013-12-31
Completion date
Unknown
Last updated
2016-06-24

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

Conditions

Arthroscopic Rotator Cuff

Brief summary

Degenerative changes of the long head of the biceps brachii (LHB) are frequent and often associated with cuff tendinopathy. The function of the LHB in the shoulder is still controversial and uncertain, whereas its function in the elbow is certain. The biceps brachii is a flexor of the elbow and supinator of the forearm. Suppression of the pathologic long head of the biceps permits pain relief and is very reliable in the literature. Two options are available for the remaining tendon : simple tenotomy or tenodesis which consists to reattach the tendon to the humerus. Our hypothesis is that there is no difference in strength or endurance of the biceps brachii after tenotomy or tenodesis of the LHB. The aim of this study was to compare the strength and the endurance of the biceps brachii during supination and flexion after tenotomy or tenodesis of the LHB. the investigators proposed a prospective and randomized study. All the patients treated in our department for an arthroscopic rotator cuff repair were included in this study after signed consent. Participants will complete isokinetic strength and endurance testing for elbow flexion and supination on the operative and nonoperative sides a minimum of 1 year after biceps tenotomy or tenodesis. The clinical evaluation included the range of motion measurement, Constant Score, Quick-DASH and SSV at 6 weeks, 3 months, 6 months and one year.

Interventions

PROCEDUREtenotomy
PROCEDUREtenodesis

Sponsors

CHU de Reims
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* surgery tenotomy or tenodesis type of the long head of the biceps (broken tendinopathy or not rotator cuff escaping a well conducted medical treatment and under a repair or cap pathology of the long head of the biceps during the arthroscopy) * Patients treated in the orthopedic service of the Reims University Hospital * Patients agreeing to participate in the research and who signed the informed consent * Major patients.

Exclusion criteria

* prior Shoulder Surgery * surgery scheduled contralateral shoulder * patient protected by law

Design outcomes

Primary

MeasureTime frame
Max Peak Torque supination1 year
Max peak Torque Flexion1 year

Countries

France

Contacts

Primary ContactXavier Ohl
xohl@chu-reims.fr326783272

Outcome results

None listed

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