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