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临床试验/NCT01183910
NCT01183910Unknown不适用

A Randomized, Double-Blind, Placebo-Controlled Study To Assess the Safety and Efficacy of a Novel Oral Natural Extract for the Treatment of Senile Purpura

Nexgen Dermatologics, Inc.2 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2008年11月最近更新:
适应症

试验速览

阶段
不适用
入组人数
75
试验地点
2
主要终点
IMPROVEMENT IN PATIENT'S SKIN APPEARANCE WITH SENILE PURPURA

研究概览

简要总结

A randomized, double-blind, placebo controlled study to assess the safety and effectiveness of a novel oral natural extract to improve the appearance of the skin of patients with senile purpura.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
盲法
Double (Participant, Investigator)

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with evidence of purpura on physical exam

排除标准

  • Preexisting condition that would not allow the patients to take oral calcium supplement

结局指标

主要结局

IMPROVEMENT IN PATIENT'S SKIN APPEARANCE WITH SENILE PURPURA

时间窗: 6 WEEKS

次要结局

  • ADVERSE EFFECTS IN PATIENTS WITH SENILE PURPURA TAKING THIS MEDICATION(6 WEEKS)

研究者

申办方类型
Industry

研究点 (2)

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