Greater Trochanteric Pain Syndrome of Both Lower Limbs Clinical Trial
— GTPSSWEXOfficial title:
Shock Wave Therapy Combined With Strengthening Exercise of Hip Abductor Muscles in the Greater Trochanteric Pain Syndrome: a Randomized Controlled Trial
Verified date | January 2024 |
Source | Foundation IRCCS San Matteo Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of this randomized controlled study is to investigate if the sequential administration of focused shock wave therapy and of a rehabilitation program based on the strengthening of gluteal muscles is more effective than a standard shock wave treatment for greater trochanteric pain syndrome
Status | Active, not recruiting |
Enrollment | 80 |
Est. completion date | February 1, 2027 |
Est. primary completion date | July 1, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: - Unilateral hip pain of four weeks or longer duration - Pain to palpation in the greater trochanteric area at physical examination - Pain in hip end-range abduction/rotation/adduction at physical examination - Gluteal tendinopathy, in absence of full thickness tears at a sonographic examination of the gluteal tendons - Adult age and written informed consent Exclusion Criteria: - No hip osteoarthritis, diagnosed according to Altman's criteria - No history of knee osteoarthritis - No history of rheumatologic diseases - No previous fractures or surgery in the affected limb - No clinical signs of lumbar radiculopathy at physical examination - No corticosteroid injections, since the onset of the current pain episode - No general contraindication to shock wave therapy (pregnancy, bleeding disorders or anticoagulant drug usage, cancer in the focal area) |
Country | Name | City | State |
---|---|---|---|
Italy | Fondazione IRCCS Policlinico San Matteo | Pavia |
Lead Sponsor | Collaborator |
---|---|
Foundation IRCCS San Matteo Hospital |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | NRS Pain | Change in lateral hip pain measured by the Numeric Rating Scale (NRS) | 6 months | |
Secondary | EQ5D Quality of life | Change in quality of life measured by EQ-5D-3L | 12 months | |
Secondary | VISA-G Disability | Change in disability measured by VISA-G questionnaire | 12 months | |
Secondary | Functional capacity (strength of gluteal muscles) | Change in functional capacity measured by MRC scale | 12 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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Reliability, Validity, and Cross-cultural Adaptation of the Turkish Version of the Victorian Institute of Sports Assessment for Gluteal Tendinopathy (VISA-G) Questionnaire
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