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Therapeutic proposal for treatment of hip Tendinopathies

Not Applicable
Recruiting
Conditions
tendinopathy
hip injuries
Registration Number
RBR-399cyrr
Lead Sponsor
Centro Universitário de Brasília - UniCEUB
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Adults diagnosed with gluteal tendinopathy through clinical and magnetic resonance imaging and who had persistent pain in the lateral region of the hip above 3 on the analogue pain scale (VAS) for more than 3 months will be admitted to the study

Exclusion Criteria

Patients diagnosed with joint pathologies such as coxarthrosis, avascular osteonecrosis of the femoral head, pain from spinal disorders or any arthropathy detected on radiographic examination were excluded from the study.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Evaluation of pain reduction verified by visual analogue pain scale and measured by pressure algometer.<br>;Evaluation of improvement in hip function measured by the Harris Hip Score and Hip Outcome Score questionnaires.
Secondary Outcome Measures
NameTimeMethod
Strength improvement, verified by e-last 02863-17-10410, portable, bluetooth dynamometer (Technology BR 10201400007232-2).<br>;Increased range of motion verified using a universal goniometer.
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