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Randomized controlled trial of abductor muscle damage in relation to the surgical approach for primary total hip replacement: minimally invasive anterolateral versus standard transgluteal approach

Not Applicable
Conditions
M16.0
M16.1
Primary coxarthrosis, bilateral
Other primary coxarthrosis
Registration Number
DRKS00000152
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
44
Inclusion Criteria

patients with primary hip arthritis,
unilateral total hip arthroplasty

Exclusion Criteria

incompliance,
patients with a heavy muscular disease,
patients with a heavy damage of the central or peripheral nervous system

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Preoperatively:<br>1. MRI to evaluate the soft tissue (cross sectional area, fatty atrophy, tendon defects, inflammation signs (fluid, bursitis, tendinitis)<br><br>3- Months follow-up<br>1. MRI - Evaluation of the soft tissue 3 months postoperatively<br><br>12- Months-follow-up<br>1. MRI - Evaluation of the soft tissue 12 months postoperatively
Secondary Outcome Measures
NameTimeMethod
Preoperatively<br>1. Abduction Test (to measure the hip abduction force)<br>2. Clinical investigation (age, weight (kg), sex, height (cm))<br>3. Clinical scores (Harris Hip, Oxf-12-Hip Score, WOMAC, Satisfaction, Pain)<br>4. Blood test (to evaluate normal values) <br><br>Postoperatively<br>1. Blood test (to measure muscle related enzymes for evaluation of muscle trauma)<br><br>3- Months follow-up<br>1. Clinical investigation (to objectify patients outcome)<br>2. Clinical scores (Harris Hip, Oxf-12-Hip Score, WOMAC, Satisfaction, Pain)<br>3. Abduction Test (to measure the hip abduction force)<br><br>12- Months follow-up<br>1. Clinical investigation (to objectify patients outcome)<br>2. Clinical scores (Harris Hip, Oxf-12-Hip Score, WOMAC, Satisfaction, Pain)<br>3. Abduction Test (to measure the hip abduction force)
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