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Effect of Ultrasound-guided Piriformis Muscle Corticosteroid Injection Versus Extracorporeal Shock Wave Therapy for Piriformis Syndrome: a Randomized Control Trial

S

Shin Kong Wu Ho-Su Memorial Hospital

Status

Completed

Conditions

Piriformis Syndrome
Corticosteroid Injection
Extracorporeal Shockwave Therapy
Therapeutic Exercise

Treatments

Procedure: Extracorporeal shockwave therapy (ESWT)
Procedure: Ultrasound-guided piriformis steroid injection

Study type

Interventional

Funder types

Other

Identifiers

NCT04684537
2021SKHADR033 (Other Grant/Funding Number)
20200715R

Details and patient eligibility

About

In this study, the investigators aim to compare the effect of extracorporeal shockwave therapy with ultrasound-guided piriformis coticosteroid injection in treatment of PS.

Full description

Piriformis syndrome (PS) is one of the common etiology of low back pain. The cause of PS is due to myofascial syndrome of piriformis muscle, leading to piriformis muscle spasm, string-like taut band, and trigger point. Consequently, it may compresses the sciatic nerve which arise from sciatic notch and passes under the piriformis muscle. Conservative treatment of PS includes therapeutic exercise, diathermy, and local steroid injection. Among them, as radiology techniques advance, ultrasound-guided piriformis injection becomes popular for diagnosis block and treatment. Nowadays, extracorporeal shockwave therapy has widely applied in musculoskeletal disease such as plantar fasciitis, tennis elbow, and calcific tendinitis of the shoulder. However, to the investigators best knowledge, there is no study comparing the therapeutic effect between local steroid injection and shockwave. In this study, the investigators aim to compare the effect of extracorporeal shockwave therapy with ultrasound-guided piriformis corticosteroid injection.

This is a randomized controlled trial. 70 participants will be randomly divided into shockwave group and injection group. The participant in the shockwave group will receive one time extracorporeal shockwave therapy, and injection group will receive one time ultrasound-guided piriformis muscle corticosteroid injection. After the intervention, participant in both groups will receive home-based stretch exercise. Evaluation will be performed at baseline, 1 week, and 5 weeks after intervention. Outcome measures include the pain visual analog scale (VAS), hip range of motion, change of pressure pain threshold, and Oswestry Disability Index (ODI).

Enrollment

70 patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age from 20 to 80
  2. Unilateral buttock involvement without leg pain or paresthesia
  3. Duration of symptoms ≥1 month
  4. Positive trigger point or taut band at piriformis muscle, confirmed by palpation and ultrasound examination
  5. Positive FAIR (flexion, adduction, internal rotation) test
  6. Positive piriformis resistive test (patient actively abducts and/or externally rotates the hip while the examiner resists these movements

Exclusion criteria

  1. Having received hip, pelvis, or lumbar spine surgery
  2. Low back pain or buttock pain due to lumbosacral spine, hip or pelvis lesion other than piriformis syndrome
  3. Having received shock wave therapy or corticosteroid injection for buttock pain within the past one month
  4. Neurologic deficit in in the lower limbs
  5. History of drug allergy to local anesthetics or corticosteroids
  6. Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 2 patient groups

Shockwave group
Active Comparator group
Description:
each subject will receive extracorporeal shockwave therapy
Treatment:
Procedure: Extracorporeal shockwave therapy (ESWT)
Injection group
Active Comparator group
Description:
each subject will receive ultrasound-guided piriformis corticosteroid injection
Treatment:
Procedure: Ultrasound-guided piriformis steroid injection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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