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Evaluation Of The Efficacy and Safety Of Tri-ActiveTM In Treatment Of Cellulite

NCT00399828 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2008-03-12

No results posted yet for this study

Summary

The purpose of this study is to assess the efficacy of device TRI-ACTIVETM (DEKA M.E.L.A., Itália)in the treatment od cellulite and body contouring.

Conditions

  • Cellulite
  • Body Contouring

Interventions

DEVICE

TRI-ACTIVE LASERDERMOLOGYTM (DEKA M.E.L.A., Itália)

Sponsors & Collaborators

  • Brazilan Center for Studies in Dermatology

    lead OTHER

Principal Investigators

  • Doris Hexsel · Brazilian Center fpr Dermatological Studies

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2006-08-31
Completion
2006-11-30

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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 NCT00399828 on ClinicalTrials.gov