NCT00904163已完成不适用
Characteristics of Adult Patients With Recessive Dystrophic Epidermolysis Bullosa
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 13
- 试验地点
- 1
研究概览
简要总结
Recessive dystrophic epidermolysis bullosa (RDEB) is a severe inherited blistering disease caused by the absence of type VII collagen. Patients with RDEB develop large, severely painful blisters and open wounds from minor trauma to their skin. We are screening RDEB subjects to determine additional characteristics of patients who survive to adulthood.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Clinical diagnosis of RDEB by local dermatologist.
- •18 years of age or more and willing to give consent.
排除标准
- •Medical instability limiting ability to travel to Stanford University Medical Center.
研究者
Alfred Lane
Professor of Dermatology and Pediatrics
Stanford University
研究点 (1)
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