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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorIstanbul University - Cerrahpasa

About this trial

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 criteria

Qualifiers

Adults aged 18 to 75 years

Buttock pain with or without radiation to the lower extremity

Ability to understand and provide written informed consent

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Ultrasound-Guided Interfascial Hydrodissection
  • Ultrasound-Guided Gluteus Maximus Dry Needling

Treatment groups

42 Participants
are divided into 2 treatment groups