NCT07526753Active, not recruitingNot Applicable
Focused Shockwave (ESWT), Radial Pressure Waves (EPAT), And Electromagnetic Transduction Therapy (EMTT) For Lower Extremity Musculoskeletal Injuries
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Mayo Clinic
- Enrollment
- 200
- Locations
- 1
- Primary Endpoint
- VAS
Study Overview
Brief Summary
The purpose of this study is to assess the efficacy of ESWT, EPAT, EMTT and the combination of these therapies in treating patients with lower extremity soft tissue, cartilage, and bone injuries.
Study Design
- Study Type
- Interventional
- Allocation
- Non Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Men and women > 18 with lower extremity musculoskeletal injury confirmed by physician
Exclusion Criteria
- •All devices: Patients with active cancer or who may be pregnant.
- •For EMTT only, patients with shrapnel, metal in the body, pacemaker, or non-MRI compatible implantable devices.
Arms & Interventions
shock wave only
Experimental
Intervention: Shock wave (Device)
shock wave + radial pressure wave
Experimental
Intervention: Shock wave (Device)
shock wave + radial pressure wave
Experimental
Intervention: Radial pressure waves (Device)
EMTT
Experimental
EMTT
Intervention: Electromagnetic transduction therapy (EMTT) (Device)
shock wave + EMTT
Experimental
Intervention: Shock wave (Device)
shock wave + EMTT
Experimental
Intervention: Electromagnetic transduction therapy (EMTT) (Device)
Outcomes
Primary Outcomes
VAS
Time Frame: initial, 6weeks, 3 months, 6 months, 1 year
Secondary Outcomes
- FAAM(baseline, 6 week, 3 month, 6 month 1 year)
Investigators
Elizabeth Bondi
Principal Investigator
Mayo Clinic
Study Sites (1)
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