An Evaluation of Kinerase Pro+Therapy Regimen Vs. Kinerase Vs. Control for the Treatment of Skin Aging

Stopped early · Phase 4

Conditions studied: Skin Aging

In brief

The purpose of this study is to compare the efficacy of the Kinerase Pro+Therapy regimen versus a single Kinerase product vs. control for the treatment of the signs of skin aging.

Key facts

Study ID

NCT00492479

Run by

Innovative Medical

Starts

2007-06-01

Expected to finish

2007-12-01

Last updated by the study team

2007-12-24

Who can join

Age: 35 and older, up to 55. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Female patients 35-55 years of age with at least moderate signs of facial aging
• Written informed consent
• Likely to complete all study visits and follow study protocol

You may not qualify if…

• Any dermatological or medical condition which would make patient participation unsafe or interfere with study outcomes or measurements
• Known hypersensitivity to any study product or their components
• Recent (within 4 weeks of baseline) surgical treatment to face (including IPL and other laser procedures)
• Prior use of anti-aging treatments for 30 days prior to study entry (physician dispensed or prescribed treatments)
• Planned facial procedures during the study (microdermabrasion, facials, etc)
• o Botox and fillers cannot be used during the trial or for 3 months prior to study entry
• Recent (within 60 days) or concurrent participation in another clinical trial
• Concomitant topical or systemic therapy that my interfere with study measurements or outcomes
• Use of any other topical photoaging/antiaging therapies during the study, other than the prescribed study regimens
• Patients who are habitual tanners (outdoors or with tanning beds) who plan on tanning during the study
• Wearing of cosmetics during study visits

Where it is running

• Steve Yoelin MD practice — Santa Ana, California, United States

Full record on ClinicalTrials.gov

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