Extracorporeal Shock Wave Treatment for Cellulite
Cellulitis
About this trial
This is an interventional treatment trial for Cellulitis focused on measuring Cellulite, Extracorporeal shock wave therapy, ESWT, Radial shock wave therapy, RSWT
Eligibility Criteria
Inclusion Criteria:
- Healthy women, < 60 years of age with cellulite grade 2-3
- Unchanged hormonal treatment for < 6 months
- Commitment to the study and ability to follow the medical directions during the study
- Signed "informed-consent" form
Exclusion Criteria:
- Previous surgery in the treated area (especially liposuction)
- Medical and/or cosmetic treatment of cellulite ongoing or within the last three months
- Infection and/or tumor diseases within the treatment area
- Anticoagulation therapy and/or hemorrhagic disorders
- Pregnancy
- Significant weight fluctuations (caused by disease or diet)
- Modified hormonal treatment
- Drugs (corticosteroids, non-steroidal antiinflammatory drugs, etc.)
- Vascular abnormalities
- Previous treatment with ESWT/RSWT
Sites / Locations
- Concept Clinic
Arms of the Study
Arm 1
Active Comparator
Radial extracorporeal shock wave therapy
All patients were treated with radial extracorporeal shock waves using the Swiss Dolorclast (Electro Medical Systems S.A., Nyon, Switzerland) and the Power+ handpiece with the 36-mm applicator. Patients were treated unilaterally with two weekly treatments for four weeks on a randomly selected leg (left or right), totaling eight treatments on the selected side. After the application of coupling gel, treatment was performed at 3.5 to 4 bar, with 15,000 impulses per session, and applied at 15 Hz. Impulses were applied homogeneously over the posterior thigh and buttock area. One patient was treated on both legs, with each leg considered an independent treatment.