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Tenotomy or Tenodesis of Long Head Biceps in Arthroscopic Rotator Cuff Repair

Sponsored by Onze Lieve Vrouwe Gasthuis

About this trial

Last updated 7 years ago

Study ID

WO 10.087

Status

Completed

Type

Interventional

Phase

N/A

Placebo

No

Accepting

50+ Years
All Sexes

Trial Timing

Ended 7 years ago

What is this trial about?

During arthroscopic rotator cuff (infraspinatus/supraspinatus) repair, biceps tendon lesions are frequently encountered. However, the most optimal treatment of the diseased long head of the biceps (LHB) tendon during rotator cuff repair remains a topic of debate: tenotomy or tenodesis. The hypothesis is that there is no difference in functional outcome between LHB tenotomy and LHB tenodesis when performed in adjunct to arthroscopic rotator cuff repair.

What are the participation requirements?

Inclusion Criteria

* Patients older than 50 years

* Degenerative rotator cuff lesion of supraspinatus/infraspinatus tendon, smaller than three centimeter.

* Patients need to be able to read and write in Dutch or English language in order to complete the questionnaires, and sign informed consent.

Exclusion Criteria

* Acute, traumatic or partial thickness rotator cuff rupture, or in case a full thickness tear is larger than 3 cm measured using an arthroscopic ruler.

* Accompanying subscapularis tendon lesion

* Hour-glass deformation bicepstendon origin or in case of accompanying subscapularis tendon rupture.

* Osteoarthritis of the glenohumeral joint

* Acromion to humeral head distance measuring 6mm or smaller.

* Prior surgery to the involved shoulder

* Dementia or inability to complete questionnaires and assessments