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CompletedNCT06783439SciaticaUpdated Nov 9, 2026

Ultrasonographic Evaluation of the Sciatic Nerve in Patients With Piriformis Syndrome

An observational study in Sciatica and Piriformis Muscle Syndrome, sponsored by Istanbul University - Cerrahpasa. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-09.

Sponsored by Istanbul University - Cerrahpasa · Observational

Updated Nov 9, 2026Enrollment updatedEligibility revised+2 moreGo to Updates ↓
Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
35
Ages
18 Years to 70 Years
Sex
All
01

Study summary

Piriformis syndrome (PS) is defined as a neuropathy of entrapment resulting from compression and irritation of the sciatic nerve at the level of the piriformis muscle (PM) at the pelvic outlet, causing sciatica radiating to the leg. The neuropathic component of PS is the compression of the sciatic nerve in or around the PM, while the primary cause of the somatic component is myofascial pain of the PM. PS accounts for 6-8% of all hip and sciatic pain cases. It is more common in middle-aged patients, and the most common etiological cause is trauma. There are various methods for the diagnosis of Piriformis Syndrome. Clinically, tenderness on palpation of the PM is the most common symptom. The FAIR test (passive flexion adduction and internal rotation of the hip), the Freiberg test (forceful internal rotation of the thigh in the supine position), the Pace test (abduction of the leg against resistance while sitting) and the Beatty maneuver (active abduction of the thigh on the affected side in the lateral decubitus position) are maneuvers that help in diagnosis. It is known that there is a delay in proximal nerve conduction (H-reflex) on the pathological side compared to the healthy side in the FAIR maneuver on EMG in PS, and it is not a sufficient test for diagnosis alone. Some studies have reported increased piriformis thickness on the pathological side in MRI. None of these clinical and imaging methods are sufficient for diagnosis alone, and today ultrasonography (US) has become one of the most important imaging methods for musculoskeletal clinicians in the diagnosis of PS. Imaging with US and the diagnostic injection test applied to the piriformis muscle with US guidance are quite important for diagnosis. There are a number of studies in the literature evaluating PM with US. These studies have shown that the piriformis muscle thickness and echogenicity increase on the pathological side. However, there is a lack of studies in the literature focusing on the evaluation of the sciatic nerve with US in patients with PS. Our aim in this study is to compare the thickness of the PM and the sciatic nerve by measuring US on both the pathological and painless sides in patients with unilateral hip pain who were diagnosed with PS clinically, to record the variations present in the sciatic nerve, and to determine whether the myofascial pain or the neuropathic component is dominant in the disease.

Read the detailed description

The sciatic nerve is the largest nerve in the body and is formed by the ventral roots of the lumbosacral plexus (L4-S3), passes through the foramen ischiadicum majus under the piriformis muscle (PM) and enters the gluteal region. It is controversial whether anatomical variations in the sciatic nerve and PM predispose to the development of Piriformis syndrome (PS). The sciatic nerve passes under the PM as a single branch in almost 90% of cases. However, there are some variations where it passes above and through the muscle or divides into tibial and peroneal branches, with one branch passing under the piriformis. There are a number of studies in the literature evaluating the PM with US. These studies have shown that the PM thickness and echogenicity increase on the pathological side. In addition, it has been mentioned that the sciatic nerve has a coarse and blurry image in patients complaining of sciatic pain. In one study, cross-sectional area measurement was performed instead of PM thickness measurement. However, this was criticized in later studies, and it was stated that it was difficult to calculate muscle volume exactly with two-dimensional US due to the irregular shape of the PM, which is anatomically pear-shaped, and that thickness measurement would provide more accurate results instead of cross-sectional area. In the first study in the literature focusing on the sciatic nerve in PS and the neuropathic pain it causes, it was found that the sciatic nerve was significantly enlarged (75%) on the symptomatic side and had decreased echogenicity in some patients when compared to healthy volunteers.

02

Conditions studied

  • Sciatica
  • Piriformis Muscle Syndrome

Keywords

  • Piriformis Muscle Syndrome
  • Sciatica
03

In context

Sciatica

149 studies on the registry are indexed under Sciatica; 31 are open to participants now.

This study's enrollment of 35 is below the median of 88 across 24 observational studies indexed under Sciatica.

Browse Sciatica studies →

Lead sponsor

Istanbul University - Cerrahpasa is the lead sponsor of 699 studies on the registry; 213 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Patients aged between 18 and 70 years with unilateral hip and/or leg pain, positive FAIR (flexion, adduction, internal rotation) test, and tenderness to palpation in the PM will be included in our study.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients aged between 18 and 70 years with unilateral hip and/or leg pain
  • Positive FAIR (flexion, adduction, internal rotation) test
  • Tenderness to palpation in the Piriformis muscle

Exclusion criteria

Exclusion Criteria:

  • Patients with a history of previous surgery involving the lumbar and/or hip region
  • A history of or infection in the pelvic region
  • (BMI) Greater than 30 kg/m2
  • Psychiatric diseases
  • Vascular disease
  • Uncontrolled diabetes, hypertension or heart failure,
  • Disc pathologies that may cause radiculopathy
  • History of rheumatic disease.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
35 participants (actual)
Target follow-up
1 Day
Patient registry
Yes

Groups and cohorts

  • Piriformis Syndrome Patients (n=20)

    Other: Ultrasound

  • Healthy Controls (n=15)

    Other: Ultrasound

Interventions

  • OtherUltrasound

    The ultrasound probe will be placed parallel to the body of the piriformis muscle on an imaginary line drawn from the sacrum to the greater trochanter of the femur. This area is also the sensitive area of the patients during the examination with pressure, and when the US probe is in this position, the subcutaneous fat tissue, gluteus maximus muscle, piriformis muscle, and the upper and lower borders of the sciatic nerve will be displayed in order from superficial to deep. First, the maximum thickness of the piriformis muscle body will be measured, then the thickness of the sciatic nerve will be measured, and the same measurements will be applied to the patient's asymptomatic hip, and the measurements will be recorded.

06

What researchers measure

Primary outcomes

  1. Tenderness in the piriformis muscle by palpation, 0-10 NRS

    Tenderness in the piriformis muscle will be assessed by palpation using the numerical scale (NRS). The numerical scale is a pain score and is evaluated between 0 and 10.

    Time frame: Day 1; single study visit

  2. Sciatic nerve thickness (measurement with US)

    Sciatic nerve thickness will be measured with ultrasound on the symptomatic and asymptomatic sides in the same patient.

    Time frame: Day 1; single study visit

  3. Piriformis muscle thickness (measurement with US)

    Piriformis muscle thickness will be measured with ultrasound on the symptomatic and asymptomatic sides in the same patient.

    Time frame: Day 1; single study visit

07

Study locations

1 site
  • İstanbul Üniversitesi - Cerrahpasa (IUC)
    Istanbul, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Dec 2024 to primary completion in Apr 2025, 4 months.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 7, 2025
First posted
Jan 20, 2025
StartActual
Dec 1, 2024
Primary completionActual
Apr 1, 2025
CompletionActual
Apr 1, 2025
Last update
Nov 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Enrollment
19→35
Nov 9, 2026
Eligibility
Revised
Nov 9, 2026
Interventions
Arms added: Piriformis Syndrome Patients (n=20)·Healthy Controls (n=15); arms removed: symptomatic hip·asymptomatic hip
Nov 9, 2026
Primary outcomes
1 edited, 2 time frame changed
What changed in the outcomes
  • ChangedBefore numeric scaleNow Tenderness in the piriformis muscle by palpation, 0-10 NRSTime frame: five months → Day 1; single study visit
  • Time frameSciatic nerve thickness (measurement with US)five months → Day 1; single study visit
  • Time framePiriformis muscle thickness (measurement with US)five months → Day 1; single study visit
Nov 9, 2026
Show all 1 update
  1. Nov 9, 2026
    Enrollment 19→35
    Eligibility Revised
    Primary outcomes 1 edited, 2 time frame changed
    What changed in the outcomes
    • ChangedBefore numeric scaleNow Tenderness in the piriformis muscle by palpation, 0-10 NRSTime frame: five months → Day 1; single study visit
    • Time frameSciatic nerve thickness (measurement with US)five months → Day 1; single study visit
    • Time framePiriformis muscle thickness (measurement with US)five months → Day 1; single study visit
    Interventions Arms added: Piriformis Syndrome Patients (n=20)·Healthy Controls (n=15); arms removed: symptomatic hip·asymptomatic hip
    + 2 other changes: verification date and description

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT06783439
Responsible party
Busra Sezer Kıral (medical doctor, Istanbul University - Cerrahpasa) — Principal investigator
First posted
Jan 20, 2025
Start date
Dec 1, 2024
Primary completion
Apr 1, 2025
Completion
Apr 1, 2025
Last update
Nov 9, 2026

Study contacts

Selim Sezikli
principal investigator · Istanbul Physical Medicine Rehabilitation Training and Research Hospital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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