NCT07198646

Brief Summary

The goal of this observational study is to evaluate the correlation between ultrasound measurements of quadratus femoris muscle thickness and ischiofemoral distance, as well as clinical parameters, with MRI measurements in patients diagnosed with ischiofemoral impingement (IFI) through MRI imaging and clinical examination. The main questions it aims to answer are: Is there a correlation between ultrasound and MRI measurements of quadratus femoris muscle thickness and ischiofemoral distance in patients with clinically and radiologically confirmed IFI? How do clinical parameters relate to ultrasound and MRI findings in these patients? What is the intra- and inter-rater reliability of ultrasound measurements for these parameters? Participants will undergo ultrasound measurement of quadratus femoris muscle thickness and ischiofemoral distance, assessment of clinical parameters related to ischiofemoral impingement, and measurements performed twice by two independent raters to assess intra- and inter-rater reliability. Researchers will compare ultrasound and MRI measurements as well as clinical parameters to determine if ultrasound can serve as a reliable and cost-effective alternative for diagnosing ischiofemoral impingement.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Oct 2024

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

October 10, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 10, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

April 10, 2025

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

September 21, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

September 30, 2025

Completed
Last Updated

September 30, 2025

Status Verified

August 1, 2024

Enrollment Period

5 months

First QC Date

September 21, 2025

Last Update Submit

September 21, 2025

Conditions

Keywords

Ischiofemoral impingement, quadratus femoris compression, hip pain diagnosis, ultrasound-MRI correlation, cost-effective imaging in hip pathology.

Outcome Measures

Primary Outcomes (1)

  • Correlation of ultrasonographic ischiofemoral space (IFS) and quadratus femoris muscle thickness with clinical and MRI parameters

    The primary outcome is to determine the relationship between ultrasonographically measured ischiofemoral space (IFS) and quadratus femoris muscle thickness with magnetic resonance imaging (MRI) findings (IFS and quadratus femoris space) and clinical parameters including pain intensity (Visual Analog Scale, VAS) and hip function (Harris Hip Score).

    Baseline (at enrollment)

Eligibility Criteria

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

1. Patients older than 18 years and younger than 65 years. 2. Patients diagnosed by MRI 3. Those with a body mass index below 25 kg/m2 4. those with hip pain or positive physical examination tests

You may qualify if:

  • Patients older than 18 years and younger than 65 years.
  • Patients diagnosed by MRI
  • Those with a body mass index below 25 kg/m2
  • those with hip pain or positive physical examination tests

You may not qualify if:

  • Sciatic nerve damage detected on EMG
  • Patients with operative ischiofemoral decompression
  • Corticosteroid or any injection to the hip in the last 3 months
  • History of peripheral nerve damage
  • Femoroacetabular impingement
  • Pregnancy
  • Malignancy
  • Inflammatory pathologies: rheumatic, septic
  • Coxarthrosis-Kelgren-Lawrence grade 3-4
  • Those who have undergone hip arthroplasty/surgery
  • Causes of lumbar radiculopathy, spondylolisthesis
  • Patients with increased femoral anteversion - patients with increased hip internal rotation (Toe-in)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Seyrantepe Hamidiye Etfal Training and Research Hospital, University of Health Sciences, Istanbul, Turkey

Istanbul, sarıyer, Turkey (Türkiye)

Location

Study Officials

  • Jülide Öncü Alptekin, Professor

    Sisli Hamidiye Etfal Training and Research Hospital

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Target Duration
8 Months
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Resident Physician, Department of Physical Medicine and Rehabilitation

Study Record Dates

First Submitted

September 21, 2025

First Posted

September 30, 2025

Study Start

October 10, 2024

Primary Completion

March 10, 2025

Study Completion

April 10, 2025

Last Updated

September 30, 2025

Record last verified: 2024-08

Data Sharing

IPD Sharing
Will not share

Locations