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A Trial of Skin Care Protocols for Facial Resurfacing

NCT01113606 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL

Last updated 2010-04-30

No results posted yet for this study

Summary

The aims of the Skin Product Assessment Research study were to (1) develop an infrastructure and process for industry-sponsored, Plastic Surgery Educational Foundation (PSEF) research in facial aesthetic surgery and (2) test the research process by comparing outcomes of the Obagi Nu-Derm System (ODNS) and conventional therapy as treatment adjuncts in ablative facial resurfacing.

Conditions

  • Facial Photo Damage
  • Periocular Fine Wrinkles
  • Perioral Fine Wrinkles

Interventions

OTHER

Obagi New-Derm System

OTHER

Standard of Care

Sponsors & Collaborators

  • The Plastic Surgery Foundation

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

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 NCT01113606 on ClinicalTrials.gov