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Comparison between two tenodesis methods in the treatment of biceps tendon and shoulder pathology.

Phase 2
Conditions
ong head of biceps tendinitis.
Bicipital tendinitis
Registration Number
IRCT201309247274N9
Lead Sponsor
Vice chancellor for research, Guilan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

All rotator cuff tore patients with at least one positive biceps tendon test (speed test, Yergoson test, active compression test or biceps instability); Inflammation, partial tear, dislocation, or SLAP lesion; Age between 14 and 65 years; No sign of extensive fatty infiltration in MRI. Exclusion criteria: History of shoulder surgery; Pain or need for surgery in both shoulders; Impossible arthroscopic repair of rotator cuff during surgery and change of arthroscopic surgery into open surgery.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain intensity. Timepoint: before, 6 months and one year after surgery. Method of measurement: Visual Analogue Scale score (VAS).
Secondary Outcome Measures
NameTimeMethod
Patient satisfaction. Timepoint: before, 6 months and one year after surgery. Method of measurement: Visual Analogue Scale score (VAS).;Functional status of shoulder. Timepoint: Before, 6 months and one year after surgery. Method of measurement: Constant score.;Functional status of shoulder. Timepoint: Before, 6 months and one year after surgery. Method of measurement: Simple Shoulder Test.
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