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Greater Trochanteric Pain SyndromeNCT07510763

Piriformis and Gluteal Muscle Thickness in Patients With Unilateral Greater Trochanteric Pain Syndrome

An observational study of Greater Trochanteric Pain Syndrome and Deep Gluteal Syndrome, run by Ankara Etlik City Hospital at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study aims to evaluate muscle thickness in patients with unilateral Greater Trochanteric Pain Syndrome using ultrasonography and to compare these findings with healthy individuals. The primary objective is to determine whether piriformis muscle thickness differs between patients and controls. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
How many people
60 participants
Where
1 siteTurkey (Türkiye)
Study dates
2 Dec 2025to 31 Mar 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Adults with unilateral Greater Trochanteric Pain Syndrome and healthy individuals without hip pain or known musculoskeletal disorders are being recruited. Participants are evaluated using ultrasonography in an outpatient clinical setting.

Who may be able to join

  • Adults aged 18 years or older
  • Diagnosis of unilateral Greater Trochanteric Pain Syndrome

Who cannot join

  • Presence of lumbar radiculopathy
  • Presence of hip or spinal osteoarthritis
  • History of lumbar spine or lower extremity surgery
  • Presence of neurological disorders affecting muscles or peripheral nerves
  • Pregnancy
  • Presence of cognitive impairment or neuropsychiatric conditions limiting participation
  • Unwillingness to participate
  • Regular participation in physical exercise (defined as more than two sessions per week)

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Ankara Etlik City Hospital

    Ankara, 06170

Other trials in Turkey (Türkiye)

About this study

Official title: Observational Assessment of Deep Gluteal Syndrome and Bilateral Piriformis, Gluteus Medius, and Gluteus Maximus Muscle Thickness Using Ultrasonography in Patients With Unilateral Greater Trochanteric Pain Syndrome

This study aims to evaluate muscle thickness in patients with unilateral Greater Trochanteric Pain Syndrome using ultrasonography and to compare these findings with healthy individuals. The primary objective is to determine whether piriformis muscle thickness differs between patients and controls. Secondary objectives include assessing gluteus medius and gluteus maximus muscle thickness, side-to-side differences in piriformis and gluteal muscle thickness, and the presence of Deep Gluteal Syndrome.

Read the detailed description

This observational cross-sectional study investigates ultrasonographic muscle morphology and associated clinical findings in patients with unilateral Greater Trochanteric Pain Syndrome (GTPS), focusing on piriformis and gluteal muscle thickness, symptom severity, and Deep Gluteal Syndrome-related findings.

Participants with unilateral GTPS and healthy controls are recruited from outpatient clinical settings. The clinical diagnosis of Greater Trochanteric Pain Syndrome is based on the presence of lateral hip pain in combination with at least two of the following findings: tenderness over the greater trochanter on palpation, pain during a 30-second single-leg stance test, or supportive ultrasonographic findings.

Ultrasonographic evaluations are performed bilaterally to measure piriformis, gluteus medius, and gluteus maximus muscle thickness. For each muscle, three measurements are obtained, and the mean value is used for analysis. Inter-side differences between affected and unaffected hips in the GTPS group and between both hips in the control group are calculated to assess asymmetry.

In the control group, the mean values of both hips are calculated and used as reference values. Comparisons are performed between affected and unaffected hips within the patient group. In addition, muscle thickness of the affected and unaffected hips in the GTPS group is compared separately with the control group mean values for each muscle. Inter-side differences in muscle thickness are also compared between patients and healthy controls. Trochanteric bursal fluid and Doppler signal changes are also evaluated using ultrasonography.

The presence of Deep Gluteal Syndrome is determined based on clinical criteria, defined as at least one clinical finding together with at least two positive standardized clinical provocation tests. Patients are categorized as Deep Gluteal Syndrome-positive or negative accordingly.

Symptom severity is assessed using the VISA-G (Victorian Institute of Sport Assessment-Gluteal) questionnaire. Correlation analyses are performed to evaluate the association between VISA-G scores and inter-side differences in muscle thickness.

Keywords
Greater Trochanteric Pain Syndrome, Musculoskeletal Ultrasound, Deep Gluteal Syndrome, Hip Pain, Muscle Thickness, Piriformis Muscle, Gluteal Muscle Thickness
Medical subject headings
Hip socket neuropathy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07510763
Study groupRoleWhat they receive
GTPS PatientsPatients with unilateral Greater Trochanteric Pain Syndrome evaluated with ultrasonography
Healthy ControlsHealthy individuals without hip pain or known musculoskeletal disorders, evaluated using ultrasonography

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Piriformis Muscle Thickness

    Comparison of piriformis muscle thickness between patients with unilateral Greater Trochanteric Pain Syndrome and healthy controls using ultrasonography

    Measured: At baseline

Secondary outcomes (6)
  1. Gluteus Medius and Gluteus Maximus Muscle Thickness

    Comparison of gluteus medius and gluteus maximus muscle thickness between patients with unilateral Greater Trochanteric Pain Syndrome and healthy controls using ultrasonography.

    Measured: At baseline

  2. Side-to-Side Muscle Thickness Comparison

    Within-group comparison of piriformis, gluteus medius, and gluteus maximus muscle thickness between affected and unaffected sides in patients with unilateral Greater Trochanteric Pain Syndrome.

    Measured: At baseline

  3. Trochanteric Bursa and Doppler Findings

    Assessment of trochanteric bursal fluid and Doppler signal changes in patients with Greater Trochanteric Pain Syndrome using ultrasonography.

    Measured: At baseline

  4. Prevalence of Deep Gluteal Syndrome

    Assessment of the presence of Deep Gluteal Syndrome in patients with Greater Trochanteric Pain Syndrome based on clinical evaluation and standardized provocation tests.

    Measured: At baseline

  5. Correlation Between VISA-G Score and Hip Muscle Thickness Asymmetry

    Correlation between VISA-G score and inter-side muscle thickness differences of piriformis, gluteus medius, and gluteus maximus measured by ultrasonography in the patient group.

    Measured: At baseline

  6. Inter-side difference in muscle thickness between patients and controls

    Comparison of inter-side differences in piriformis, gluteus medius, and gluteus maximus muscle thickness between patients with unilateral Greater Trochanteric Pain Syndrome and healthy controls using ultrasonography

    Measured: At baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Apr 2026
  2. Study start2 Dec 2025
  3. Primary completion31 Mar 2026
  4. Study completion31 Mar 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
60 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07510763
Sponsor's protocol ID
AEŞH-BADEK1-2025-015
Status last verified
Mar 2026
First submitted
27 Mar 2026
Last updated
13 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Firat A, Veizi E, Karaman Y, Alkan H, Sahin A, Tolunay T, Kilicarslan K. Unrepaired Trochanteric Bursae as a Risk Factor for Deep Gluteal Syndrome After Total Hip Arthroplasty: A Prospective Randomized Controlled Trial. J Arthroplasty. 2024 Apr;39(4):1025-1030. doi: 10.1016/j.arth.2023.10.049. Epub 2023 Nov 2.

    PubMed 37924993
  • Othman IK, Raj NB, Siew Kuan C, Sidek S, Wong LS, Djearamane S, Loganathan A, Selvaraj S. Association of Piriformis Thickness, Hip Muscle Strength, and Low Back Pain Patients with and without Piriformis Syndrome in Malaysia. Life (Basel). 2023 May 18;13(5):1208. doi: 10.3390/life13051208.

    PubMed 37240853
  • Whittaker JL, Emery CA. Sonographic measures of the gluteus medius, gluteus minimus, and vastus medialis muscles. J Orthop Sports Phys Ther. 2014 Aug;44(8):627-32. doi: 10.2519/jospt.2014.5315. Epub 2014 Jul 16.

    PubMed 25029916
  • Geler Kulcu D. Deep Gluteal syndrome: An underestimated cause of posterior hip pain. Turk J Phys Med Rehabil. 2024 Feb 1;70(1):4-16. doi: 10.5606/tftrd.2024.14668. eCollection 2024 Mar.

    PubMed 38549816
  • Speers CJ, Bhogal GS. Greater trochanteric pain syndrome: a review of diagnosis and management in general practice. Br J Gen Pract. 2017 Oct;67(663):479-480. doi: 10.3399/bjgp17X693041. No abstract available.

    PubMed 28963433

Questions about this trial

What is this clinical trial studying?

An observational study of Greater Trochanteric Pain Syndrome and Deep Gluteal Syndrome, run by Ankara Etlik City Hospital at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 13 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Piriformis Muscle Thickness (time frame: At baseline). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07510763, which also lists 5 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Apr 2026.

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