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International CoolSculpting: Study to Evaluate Patient Satisfaction for Non-Invasive Fat Reduction in Abdomen and/or Flanks (iCOOL)

NCT03909100 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2023-06-27

Study results available
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Summary

This study aims to generate data that conveys participant's experiences such as their overall satisfaction with the CoolSculpting® treatment for their belly and love handles. By doing this, the study will provide insights for doctors to better inform participants about the expected outcomes.

Conditions

  • Non-invasive Fat Reduction

Interventions

DEVICE

CoolSculpting® System

A treatment session is comprised of timed segments of cooling (treatment cycles) followed by 2 minutes of manual massage.

Sponsors & Collaborators

  • Allergan

    lead INDUSTRY

Principal Investigators

  • Esther Jo · Allergan

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2019-07-29
Primary Completion
2020-02-28
Completion
2020-02-28
FDA Device
Yes

Countries

  • Australia
  • Canada
  • Singapore
  • United Kingdom

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 NCT03909100 on ClinicalTrials.gov