MedTrace Logo

Evaluation of Fractional Bipolar Radiofrequency for the Treatment of Striae

NCT01788748 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2013-12-31

No results posted yet for this study

Summary

This is an interventional open prospective randomized study, done in two sites.

The main purpose of this study is to evaluate the efficacy of the combination of bipolar radiofrequency potentiated by an infrared light followed by fractional bipolar radiofrequency for the treatment of striae on the abdomen.

In order to have a more complete and accurate study, each technology will also be evaluated separately. This will allow the comparison of the effect of each treatment, in monotherapy or combined.

Conditions

  • Striae

Interventions

DEVICE

bipolar radiofrequency and infrared

DEVICE

fractional bipolar radiofrequency

Sponsors & Collaborators

  • Candela France

    lead INDUSTRY

Principal Investigators

  • Thierry Passeron, Pr · Hopital Archet II, service de Dermatologie

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2013-11-30
Completion
2013-11-30

Countries

  • France

Study Locations

More Related Trials

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 NCT01788748 on ClinicalTrials.gov