跳至主要内容
临床试验/NCT00492479
NCT00492479终止4 期

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

Innovative Medical2 个研究点 分布在 1 个国家开始时间: 2007年6月最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
终止
试验地点
2

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Single

入排标准

年龄范围
35 Years 至 55 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

研究者

申办方类型
Industry

研究点 (2)

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