IRCT201702231165N18已完成1 期
Evaluation of efficacy and safety of topical naloxone in control of chronic pruritus in patients with neurodermatitis
Baqiyatallah University of medical sciences0 个研究点目标入组 70 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 70
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 70 years 至 30 years（—）
- 性别
- All
入选标准
- •The patient has no addiction; have not been treated with any form of topical steroids; diagnosis of neurodermitis has been confirmed by a physician; the content form should have been completed by the patient; age between 25 and 65 years; have no other skin disorders; accessible at all times during the trial; do not leave the treatment after one week; do not have allergy to the medication. Exclusion criteria: when disease become uncontrollable; severe reaction or allergy to the medication; patients’ age less the 25 and more than 65 years
排除标准
- 未提供
研究者
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