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Dermal Cryotherapy in Patients Undergoing Abdominoplasty

NCT02763306 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2021-03-29

No results posted yet for this study

Summary

A prospective, interventional, single-arm study to evaluate histologic changes in skin following cryotherapy with the study device.

Conditions

  • Skin Laxity

Interventions

DEVICE

Dermal Cooling System

Treatment with dermal cooling system.

Sponsors & Collaborators

  • R2 Dermatology

    lead INDUSTRY

Principal Investigators

  • David Kaufman, MD · Kaufman Plastic Surgery

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2017-04-30
Completion
2017-04-30
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 NCT02763306 on ClinicalTrials.gov