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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00492479
Recruitment Status : Terminated
First Posted : June 27, 2007
Last Update Posted : December 24, 2007
Information provided by:
Innovative Medical

Brief Summary:
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.

Condition or disease Intervention/treatment Phase
Skin Aging Drug: Kinerase Pro+Therapy Line day repair, serum, night repair Drug: Kinerase Pro+Therapy Line Ultra rich day repair Drug: LubriDerm Phase 4

Study Type : Interventional  (Clinical Trial)
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single
Study Start Date : June 2007
Actual Study Completion Date : December 2007

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Skin Aging
U.S. FDA Resources

Information from the National Library of Medicine

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Ages Eligible for Study:   35 Years to 55 Years   (Adult)
Sexes Eligible for Study:   Female

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00492479

United States, California
Steve Yoelin MD practice
Santa Ana, California, United States, 92701
Sponsors and Collaborators
Innovative Medical
Principal Investigator: Steven Yoelin, MD Private Practice Identifier: NCT00492479     History of Changes
Other Study ID Numbers: 5314
First Posted: June 27, 2007    Key Record Dates
Last Update Posted: December 24, 2007
Last Verified: December 2007

Additional relevant MeSH terms:
Plant Growth Regulators
Growth Substances
Physiological Effects of Drugs