EUCTR2016-003753-14-FR进行中（未招募）1 期
CERVICAL PREPARATION UNDER PARACERVICAL BLOCK FOR THE ABORTION OF FIRST TRIMESTER: RANDOMIZED TRIAL - BPCE
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 1
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
入选标准
- •Women aged 18 or over;
- •Woman with a single intrauterine pregnancy, the term is between 6SA and strictly less than 14 weeks on the day of the abortion, estimated by ultrasound measurement of the cranio-caudal length of between 5 and 84 millimeters;
- •Female looking for abortions under local anesthesia;
- •Women who have signed a written informed consent and agreeing to abide by the instructions of the protocol.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 110
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Woman wishing to interrupt her participation in the study before the end;
- •Woman for whom surgery was not performed (no show the patient the day of surgery, miscarriage before the operation).
- •Women who have not followed the protocol (not taken for a product).
研究者
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