Clinical Study to Evaluate the Safety and Efficacy of the Vela100
NCT01026441 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2011-05-05
Summary
This study is intended to test the safety of the Vela100 device when used for treatment for cellulite and circumference temporary reduction.
Conditions
- Cellulite Reduction
- Circumference Reduction
Interventions
- DEVICE
-
Vela100 (Aesthetic)
6 treatments once a week
Sponsors & Collaborators
-
Syneron Medical
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 21 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2008-10-31
- Primary Completion
- 2008-10-31
- Completion
- 2008-10-31
Countries
- United States
Study Locations
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