NCT07431138

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
68

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 14, 2026

Completed
29 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 12, 2026

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 17, 2026

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

February 19, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

February 24, 2026

Completed
Last Updated

February 24, 2026

Status Verified

February 1, 2026

Enrollment Period

29 days

First QC Date

February 19, 2026

Last Update Submit

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.

Diagnostic Test: Shear-Wave Elastography (Ultrasound)

Interventions

Non-interventional ultrasound performed during routine follow-up.

Postoperative Follow-up Cohort

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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)

Location

MeSH Terms

Interventions

Ultrasonography

Intervention Hierarchy (Ancestors)

Diagnostic ImagingDiagnostic Techniques and ProceduresDiagnosis

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.

Locations