跳至主要内容
临床试验/NCT06894732
NCT06894732尚未招募不适用

To Study the Safety and Efficacy of Disposable Cyclone Ring in Artificial Abortion

Peking Union Medical College Hospital1 个研究点 分布在 1 个国家目标入组 332 人开始时间: 2025年3月20日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
332
试验地点
1
主要终点
Cervical dilation rate (e.g. %)

研究概览

简要总结

The purpose of this study is to compare the two surgical methods of surgical rotation abortion and surgical negative pressure uterine aspiration with the termination of pregnancy. which one can better protect female fertility; To understand the impact of both surgical approaches on the long-term prognosis of patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Age: 20-40 years old, planning to terminate pregnancy; 2) Menopause time≤ 56 days (8 weeks); 3) Ultrasound examination showed early pregnancy in utero, and the average diameter of the fetal sac was 1-3cm; 4) According to the requirements of clinical operation standards, the preoperative examination, laboratory results and surgical indicators are normal 5) The subject was conscious, had good compliance, agreed to participate in the trial, and voluntarily signed the informed consent form

排除标准

  • According to the requirements of clinical practice, there are contraindications to induced abortion; 2) The number of previous induced abortions ≥2 times; 3) Diseases affecting uterine cavity morphology such as uterine malformations and uterine fibroids; 4) History of uterine surgery: such as submucosal myomectomy history, mediastinal resection history, uterine adhesion-separation history; 5) Unable to sign the informed consent; 6) Other conditions that the investigator considers inappropriate to participate in this clinical study.

结局指标

主要结局

Cervical dilation rate (e.g. %)

时间窗: 30

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

To Study the Safety and Efficacy of Disposable... | 临床试验