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CoolSculpting of the Flank With Alternate Treatment Parameters

NCT02081196 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2021-03-01

Study results available
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Summary

The purpose of this study is to evaluate the safety and efficacy of non-invasive subcutaneous fat layer reduction with an alternative treatment parameter.

Conditions

  • Body Fat Disorder

Interventions

DEVICE

The Zeltiq CoolSculpting System

Non-invasive cooling is applied to the treatment area with a defined cooling rate and duration.

Sponsors & Collaborators

  • Zeltiq Aesthetics

    lead INDUSTRY

Principal Investigators

  • Suzanne Kilmer, MD · Laser and Skin Surgery Center of Northern California

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2014-02-18
Primary Completion
2014-06-27
Completion
2014-06-27
FDA Device
Yes

Countries

  • United States
  • Canada

Study Locations

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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 NCT02081196 on ClinicalTrials.gov