JPRN-UMIN000049894已完成Unknown
Safety evaluation of endometrial biopsy for ERA/EMMA/ALICE analyses - Safety evaluation of endometrial biopsy for ERA/EMMA/ALICE analyses
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 入组人数
- 10
研究概览
简要总结
We recruited and completed 10 subjects as scheduled. Main out come measured was presence of absence of adverse events. We did not observe any adverse event. Secondary endpoints was percentage of defective specimens which incompatible for analysis. There was no defective specimen and we could obtain result from all specimens from all 10 participants.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18years-old 至 43years-old（—）
- 性别
- Female
入选标准
- 未提供
排除标准
- •(1)Patient who dose not fulfill inclusion criteria (2)Patient who dose not agree with study participation (3)Patient who are receiving treatment for endometrial hyperplasia or endometrial cancer (4)Patient who have difficulty for endometrial biopsy due to congenital mullerian duct anomaly, Bleeding tendency and/or who requires hospital admission for anesthesia. (5)Patient who are pregnant or suspicious of pregnancy (6)Patient who have psychosomatic problem and have been decided to difficult to participant.
研究者
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