EUCTR2008-006004-36-DK进行中（未招募）不适用
Efficacy and tolerability of captopril ointment 0,1%, 0,3% and 1,0% in psoriasis vulgaris. A randomised, double-blind, placebocontrolled, doseescalating, intra-individual clinical study
ACE ApS0 个研究点开始时间: 2008年11月4日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Patients with psoriasis vulgaris
- •Age 18-80 (both included)
- •White (caucasian)
- •Normal weight
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Active psoriasis on test plaques reguiring dermatological treatment
- •Other skin disease (e.g. contact allegy, atopic dermatitis, urticaria)
- •Dermatological lighttreatment or use of solarium 4 weeks prior to the trial.
- •Start of systemic treatment prior to study start which can influence on the test plaques. Stabil systemic treatment started 4 month prior to study start are allowed as well as local treatment on other plaques than test plaques during the trial.
- •Known hypersensitivity to any constituents or active ingredients in the amounts present in the trial medication.
- •Known coronary heart disease.
- •Alcohol abuse or other type of abuse or dependency.
- •Participation in a clinical trial within 30 days prior to inclusion in this trial.
- •Lack of use of safe anticontraception.
研究者
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