Functional Change With MMS
NCT04506502 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16
Last updated 2025-05-16
Summary
Evaluate the safety and efficacy of magnetic muscle stimulation (MMS) of abdominal muscle.
Conditions
- Muscle Weakness
Interventions
- DEVICE
-
The ZELTIQ System
The MMS device will be used to perform the treatments.
Sponsors & Collaborators
-
Zeltiq Aesthetics
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- OTHER
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 22 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2020-03-04
- Primary Completion
- 2021-05-18
- Completion
- 2021-07-06
- FDA Device
- Yes
Countries
- United States
Study Locations
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