IRCT20130921014727N7已完成4 期
The Pilot Study of Efficacy and Safety of Cyproheptadine in Pulmonary Arterial Hypertension Patients in Massih Daneshvari Hospital
Faculty of Pharmacy, Shahid Behesti University of Medical Sciences0 个研究点目标入组 12 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 12
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
- 18 years 至 75 years（—）
- 性别
- All
入选标准
- •patients with mean pulmonary arterial pressure (mPAP) =25 mmHg (confirmed by catheterization at diagnosis time) and symptomatic pulmonary arterial hypertension (PAH) diagnosis
- •functional class (FC) II or III according to the world health organization classification
- •ages between 18 and 75 years old
- •6-minute walk test (6-MWT) distance of 50 to 450 m
- •patients receiving stable treatments for PAH, the phosphodiesterase-5 inhibitors or the endothelin-receptor antagonist (bosentan) or both at a dose, and were being stable clinical and hemodynamical status for at least 3 months before randomization
- •use of anticoagulants, calcium channel blocker and diuretics will be allowed when the medicine or dosage was unchanged for at least last 3 months
排除标准
- •SSRIs, CCBs, MAOIs, sedatives, hypnotics, and alcohol consumers
- •patients who sleepiness and drowsiness are associated with hazards in their jobs
- •pregnancy and lactation
- •symptomatic prostate hypertrophy
- •CKD ( SCr.2.5, proteinuria>500mg/d)
- •angle-closure glaucoma
研究者
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