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The INFORM Study: Rotational Fractional Resection for Submental Contouring

NCT03853980 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 21

Last updated 2020-03-06

No results posted yet for this study

Summary

Efficacy and safety of Rotational Fractional Resection (skin resection) in patients with moderate to severe submental skin laxity.

Conditions

  • Skin Laxity

Interventions

DEVICE

Focal Contouring System

Single treatment of skin resection (removal of loose skin)

Sponsors & Collaborators

  • Recros Medica, Inc.

    lead INDUSTRY

Principal Investigators

  • Robin McIntosh · Recros Medica

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
30 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-03-18
Primary Completion
2020-10-31
Completion
2020-10-31
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 NCT03853980 on ClinicalTrials.gov