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Piriformis Syndrome; Extracorporeal Shock Wave Therapy and Dry Needling

Not Applicable
Completed
Conditions
Piriformis Syndrome
Extracorporeal Shock Wave Therapy
Interventions
Other: Dry needling+stretching exercises
Other: 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
Inclusion Criteria
  • >18 years
  • Complaint for more than 3 months
Exclusion Criteria
  • 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
GroupInterventionDescription
Dry needlingDry needling+stretching exercisesThe 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 groupESWT+stretching exercisesPatients 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
NameTimeMethod
Visual analog scale (VAS) score7 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
NameTimeMethod

Trial Locations

Locations (1)

Burak Tayyip Dede

🇹🇷

Istanbul, Turkey

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