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Long-term Follow-up Study of the truSculpt Radiofrequency Device for Circumferential Reduction

NCT03428243 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 14

Last updated 2018-03-20

No results posted yet for this study

Summary

A long-term follow-up study to evaluate the safety and efficacy of the Cutera truSculpt radiofrequency device for circumferential reduction.

Conditions

  • Abdominal Fat

Interventions

DEVICE

truSculpt

Device comparison of Circumference measurement at Baseline vs 18 months post treatment

Sponsors & Collaborators

  • Cutera Inc.

    lead INDUSTRY

Principal Investigators

  • Stephen Ronan, MD · Principal Investigator

Eligibility

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

Timeline & Regulatory

Start
2017-07-12
Primary Completion
2017-11-06
Completion
2017-12-01
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 NCT03428243 on ClinicalTrials.gov