Piriformis Syndrome; Extracorporeal Shock Wave Therapy and Dry Needling
- Conditions
- Piriformis SyndromeExtracorporeal Shock Wave Therapy
- Interventions
- Other: Dry needling+stretching exercisesOther: ESWT+stretching exercises
- Registration Number
- NCT06530862
- Lead Sponsor
- Istanbul Training and Research Hospital
- Brief Summary
This study is being conducted on patients with piriformis syndrome. Patients are divided into two groups by list randomization method: Extracorporeal shock wave therapy (ESWT) group and Dry neddling (DN) group. Both groups of patients agreed to perform basic stretching exercises. The ESWT group received 3 sessions of radial ESWT, 1 session per week. The DN group received 3 sessions of ultrasound-guided needling, 1 session per week. Clinical evaluations of the participants were performed at the beginning of treatment, 1 month, and 3 months after treatment.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 44
- >18 years
- Complaint for more than 3 months
- disc pathologies according to radiological imaging
- hip joint and soft tissue pathologies
- recent history of trauma, history of surgery in the lumbar and hip region
- history of rheumatologic disease
- history of polyneuropathy
- history of sciatic nerve injury
- history of malignancy
- opioid analgesia or corticosteroid intervention for pain in the last month
- patients receive another treatment during the study
- Having a contraindication for DN treatment or ESWT treatment
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Dry needling Dry needling+stretching exercises The piriformis muscle of the patients in the group will be dry needled with 0.6\*80 mm acupuncture needles under ultrasound guidance for 3 sessions at one week intervals. ESWT group ESWT+stretching exercises Patients in this group received three sessions of ESWT at an energy density of 4 bars and a frequency of 2,000 shocks/min at 5 Hz for three weeks, each session once a week.
- Primary Outcome Measures
Name Time Method Visual analog scale (VAS) score 7 months Pain was evaluated with a Visual analog scale (VAS) score
Lower extremity functiunal scale (LEFS) 7 months Pain was evaluated with a Lower extremity functiunal scale (LEFS (minimum=0, maximum=80)) The higher the score, the better the result
Oswestry disability index (ODI) 7 months Pain was evaluated with a Oswestry disability index (ODI (minimum=0, maximum=60))The lower the score the better the result
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Burak Tayyip Dede
🇹🇷Istanbul, Turkey