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Multi-Center Pilot Study of Cutera truSculpt Device

NCT03782545 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2023-09-13

Study results available
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Summary

Exploratory study to evaluate the safety, efficacy and ergonomics of Cutera truSculpt device.

Conditions

  • Treatment for Cellulite on the Stomach and Flanks

Interventions

DEVICE

Cutera truSculpt Device

The Cutera truSculpt Device uses radio frequency (RF) energy to provide topical heating for the purpose of elevating tissue temperature for the treatment of selected medical conditions, such as temporary reduction in the appearance of cellulite.

Sponsors & Collaborators

  • Cutera Inc.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2018-05-11
Primary Completion
2018-12-19
Completion
2018-12-19
FDA Device
Yes

Countries

  • United States

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 NCT03782545 on ClinicalTrials.gov