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Comparison of two different types of injectable medications in the treatment of biceps tendinopathy under ultrasound guidance

Phase 2
Conditions
Health Condition 1: M678- Other specified disorders of synovium and tendon
Registration Number
CTRI/2023/07/054974
Lead Sponsor
Regional Institute of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Clinical and Ultrasound diagnosed cases of bicipital tendinosis

2.Age between 18 to 60 years of age

3.Failure of conservative treatment > 3months

4.Willingness to comply with treatment and follow up assessment

Exclusion Criteria

1.Local injection within 6 weeks

2.Local infection at the site of injection

3.Evidence of rotator cuff tear, GHJ deformity or rupture of LHB tendon on MRI

4.Uncontrolled systemic disease

5.Thrombocytopenia ( <1.5 lakhs/cumm)

6.Bleeding disorder

7.Pregnancy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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