Pivotal Study of the truSculpt Radiofrequency Device for Circumferential Reduction

NCT02873104 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2018-02-28

Study results available
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Summary

To evaluate the safety and efficacy of the Cutera truSculpt radiofrequency device for circumferential reduction.

Conditions

  • Abdominal Fat

Interventions

DEVICE

truSculpt rf device

radiofrequency device

Sponsors & Collaborators

  • Cutera Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
24 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-03-31
Primary Completion
2016-09-30
Completion
2016-09-30
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 NCT02873104 on ClinicalTrials.gov