CoolSculpting and EMS for the Abdomen

NCT03738891 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2025-05-16

Study results available
· View outcomes & findings →

Summary

Evaluate the use of Electromagnetic Muscle Stimulation as an adjunctive treatment to CoolSculpting.

Conditions

  • Body Fat Disorder

Interventions

DEVICE

Zeltiq CoolSculpting System alone

The CoolSculpting System will be used to perform the treatments in Cohort 3.

DEVICE

Electromagnetic Muscle Stimulation alone

The EMS device(s) alone are used in Cohort 1.

DEVICE

EMS followed by CoolSculping

Cohort 2 group will be treated with EMS followed by CoolSculpting

DEVICE

CoolSculpting followed by EMS

Cohort 4 will be treated first with CoolSculpting, followed by EMS.

Sponsors & Collaborators

  • Zeltiq Aesthetics

    lead INDUSTRY

Principal Investigators

  • Kerrie Jiang, NP · Zeltiq Aesthetics

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-11-07
Primary Completion
2019-09-09
Completion
2019-09-09
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03738891 on ClinicalTrials.gov