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
适应症
干预措施
试验速览
- 阶段
- 不适用
- 入组人数
- 75
- 试验地点
- 1
- 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
- 是
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
研究组 & 干预措施
Nutraceutical
Active Comparator
Patients take a novel, natural nutraceutical product to improve the appearance of the skin of patients with senile purpura
干预措施: Citrus Bioflavanoid Blend (Dietary Supplement)
Calcium carbonate placebo pill
Placebo Comparator
Placebo medication to treat the appearance of the skin in patients with senile purpura
干预措施: Calcium Carbonate (Dietary 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
研究点 (1)
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