跳至主要内容
临床试验/JPRN-UMIN000053599
JPRN-UMIN000053599尚未招募Unknown

Efficacy evaluation of endometrial biopsy for ERA/EMMA/ALICE analyses - Efficacy evaluation of endometrial biopsy for ERA/EMMA/ALICE analyses

Tohoku university0 个研究点目标入组 50 人开始时间: 2024年2月13日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
入组人数
50

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
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

相似试验