EUCTR2005-000963-25-Outside-EU/EEA进行中（未招募）不适用
A Multicenter, Long-Term Extension Study to Assess Safety of Oral Sildenafil in the Treatment of Subjects Who Have Completed Study A1481131 - N/A
Pfizer Limited, Ramsgate Road, Sandwich, Kent, UK0 个研究点目标入组 220 人开始时间: 2012年3月7日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 220
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
- •· Pediatric subjects, who enrolled in and completed Study A1481131;
- •· Females of childbearing potential who are sexually active must be practicing a suitable method of birth control so that in the opinion of the investigator, they will not become pregnant during the study; and
- •· The investigator must obtain written informed consent and assent where applicable before the subject is considered for enrollment in Study A1481156. The inclusion of a subject more than once in the same clinical trial is not permissible.
- •All inclusion criteria must be adhered to.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 217
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 3
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Pediatric subjects, who did not complete Study A1481131.
- •Subjects with known hereditary degenerative retinal disorders (such as retinitis
- •pigmentosa) or history of non-arteritic anterior ischemic optic neuropathy (NAION).
- •The exclusion criteria must be adhered to.
研究者
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