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Phase 2 N=24 Randomized Triple-blind Treatment

Comparison of Retinol 1.0% and Tretinoin 0.02% in the Treatment of Moderate to Severe Photodamage and Wrinkles

Photodamaged Skin · Wrinkles

Enrolled (actual)
24
Serious AEs
12.5%
Results posted
Aug 2013
Primary outcome: Primary: Global Photodamage Severity — 4.8; 5.45 units on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Retinol (Drug); Tretinoin (Drug)
Age
Adult, Older Adult · 35+ yrs
Sex
All
Sponsor
Johns Hopkins University
Primary completion
Dec 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Global Photodamage Severity
4.8; 5.45

Summary

The purpose of this study is to assess the comparative efficacy of retinol 1.0% and tretinoin 0.02% in minimizing wrinkles, discoloration, roughness, and other signs of moderate to severe photodamage. Our hypothesis is that both products will be of comparable benefit.

Eligibility Criteria

Inclusion Criteria

  • Age 35 or over
  • Moderate to severe photodamage

Exclusion Criteria

  • History of facial cosmetic surgery, facial resurfacing procedures, deep peels, or facial fillers
  • History of keloids or hypertrophic scars
  • Use of oral steroids or oral retinoids (such as Accutane) in past 6 months
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01283464). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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