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Clinical Trials in Turkey / NCT07326982
Starting soon Not applicable

Ultrasound-Guided Interfascial Hydrodissection for Gluteal Myofascial Pain in Piriformis Syndrome: A Prospective Study

NCT07326982 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-26
Last updated
2026-03-13

Condition(s) studied

Piriformis SyndromeGluteus Maximus Myofascial Pain

Investigational drug(s) / intervention(s)

Ultrasound-Guided Interfascial HydrodissectionUltrasound-Guided Gluteus Maximus Dry Needling

Ultrasound-Guided Interfascial Hydrodissection: Ultrasound-guided interfascial hydrodissection is performed in the interfascial plane between the gluteus maximus and piriformis muscles.

Ultrasound-Guided Gluteus Maximus Dry Needling: Ultrasound-guided dry needling is performed on the gluteus maximus muscle without fluid administration.

Study summary

This randomized, double-blind prospective trial investigates whether ultrasound-guided interfascial hydrodissection using 10% dextrose is more effective than dry needling in treating gluteal myofascial pain coexisting with piriformis syndrome. Following diagnostic piriformis injection response, eligible patients will be randomized into two treatment arms and followed at 1 hour, 1 week, 1 month, and 3 months. The primary hypothesis is that interfascial hydrodissection will provide superior long-term analgesic outcomes due to fascial separation, neuromodulation, and nociceptor suppression.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18 to 75 years * Buttock pain with or without radiation to the lower extremity * Ability to understand and provide written informed consent Exclusion Criteria: * Active lumbar radiculopathy * History of hip joint pathology or prior hip surgery * Previous injection or dry needling treatment to the gluteal region within the last 3 months * Coagulation disorders or use of anticoagulant therapy * Pregnancy * Local infection at the injection site * Inability to complete the study protocol or attend follow-up visits.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Istanbul University-Cerrahpaşa, Cerrahpaşa Faculty of Medicine Istanbul Istanbul

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07326982 on ClinicalTrials.gov ↗ ← All trials in Turkey