Role of Iliotibial Band Stiffness in Perceived Leg Length Discrepancy After Total Hip Arthroplasty
The Role of Iliotibial Band Stiffness Assessed by Shear-Wave Elastography in Objective and Perceived Leg Length Discrepancy After Total Hip Arthroplasty
1 other identifier
observational
68
1 country
1
Brief Summary
Patients undergoing total hip arthroplasty (THA) may experience objective or perceived leg length discrepancy (LLD/PLLD), which can negatively affect gait, pelvic balance, and patient satisfaction. The iliotibial band (ITB) plays a critical role in lateral thigh tension transmission, and alterations in its stiffness may influence the perception of limb length discrepancy. Shear-wave elastography (SWE) is a noninvasive ultrasound-based technique that enables quantitative assessment of soft tissue stiffness. This cross-sectional observational study aims to investigate the relationship between ITB stiffness measured by SWE and both radiographic and perceived leg length discrepancy in adult patients who underwent unilateral primary THA at least 12 months previously.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jan 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 14, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 12, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
February 17, 2026
CompletedFirst Submitted
Initial submission to the registry
February 19, 2026
CompletedFirst Posted
Study publicly available on registry
February 24, 2026
CompletedFebruary 24, 2026
February 1, 2026
29 days
February 19, 2026
February 19, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
Harris Hip Score
At least 12 months postoperatively
Oxford Hip Score
At least 12 months postoperatively
HOOS score
Hip Disability and Osteoarthritis Outcome Score
At least 12 months postoperatively
Secondary Outcomes (1)
leg length difference
At least 12 months postoperatively
Other Outcomes (1)
iliotibial band tension-elastogram
At least 12 months postoperatively
Study Arms (1)
Postoperative Follow-up Cohort
Patients who underwent surgery and were followed as part of routine postoperative care. Clinical scores and radiographic assessments were recorded during follow-up. Non-interventional ultrasound evaluation was performed in patients who had completed at least 12 months after surgery; some patients were assessed at longer postoperative intervals.
Interventions
Non-interventional ultrasound performed during routine follow-up.
Eligibility Criteria
Patients who underwent total hip arthroplasty and had a minimum follow-up of at least 1 year were included in the study.
You may qualify if:
- Age between 18 and 90 years History of unilateral primary TKA, with no prior revision surgery At least 12 months after surgery and returned to functional weight-bearing No use of walking aids, or use of a cane only for outdoor ambulation
You may not qualify if:
- Bilateral TKA or severe osteoarthritis in the contralateral hip History of femoral, tibial, or hip surgery resulting in limb length-altering deformity Significant scoliosis (\>20° Cobb angle) or pelvic obliquity \>5° Neurological disorders (e.g., severe polyneuropathy, hemiparesis) History of lateral thigh surgery (e.g., IT band release, TFL surgery) Body mass index (BMI) \>40 (may reduce the reliability of SWE measurements) Suspected prosthetic joint infection or implant instability
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ankara Etlik City Hospital
Ankara, Yenimahalle, 06170, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 12 Months
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 19, 2026
First Posted
February 24, 2026
Study Start
January 14, 2026
Primary Completion
February 12, 2026
Study Completion
February 17, 2026
Last Updated
February 24, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared.