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In-vivo Analysis of a Fractional CO2 Laser System (eMatrixCO2) Intended for Treatment of Soft Tissue

NCT01026662 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 5

Last updated 2014-12-02

No results posted yet for this study

Summary

This study will:

Evaluate the in vivo effects of treatment with eMatrixCO2 and to determine the dynamics of their development over time following treatment.

Conditions

  • Abdominoplasty

Interventions

PROCEDURE

Ablation and skin resurfacing

Subjects will receive treatment on the abdomen at different timepoints prior to a scheduled abdominoplasty. Following tissues excision samples of the treated tissue will be taken for analysis.

DEVICE

eMatrixCO2

Sponsors & Collaborators

  • Syneron Medical

    lead INDUSTRY

Eligibility

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

Timeline & Regulatory

Start
2009-11-30
Primary Completion
2010-04-30

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 NCT01026662 on ClinicalTrials.gov