NL-OMON21396Other不适用
Genetics of pelvic organ prolapse; identification of specific gene defects in patients and their family members.
适应症
试验速览
- 阶段
- 不适用
- 状态
- Other
- 发起方
- one
- 入组人数
- 50
研究概览
简要总结
/A
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •First and second degree relatives of patients with COL3A1 polymorphism.
排除标准
- •1. Genetic diseases with a known increased risk of POP (such as Ehlers Danlos, Marfan and Steinert’s disease);
- •2. Problems with regards to the patient’s understanding of the study;
研究者
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