NCT00492479TerminatedPhase 4
An Evaluation of Kinerase Pro+Therapy Regimen Vs. Kinerase Vs. Control for the Treatment of Skin Aging
Conditions
Drugs
Trial Snapshot
- Phase
- Phase 4
- Status
- Terminated
- Sponsor
- Innovative Medical
- Locations
- 1
Study Overview
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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Masking
- Single
Eligibility Criteria
- Ages
- 35 Years to 55 Years (Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
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
Investigators
Study Sites (1)
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