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临床试验/ChiCTR1900023198
ChiCTR1900023198招募中Unknown

The incidence of intrauterine adhesion after ultrasound-guided manual vacuum aspiration (USG-MVA): A prospective randomized controlled trial

未提供1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2019年6月1日最近更新:

试验速览

阶段
Unknown
状态
招募中
入组人数
300
试验地点
1
主要终点
the incidence of intrauterine adhesion

研究概览

简要总结

To determine the incidence of intrauterine adhesion or Ashermans syndrome after ultrasound guided mannual vacuum aspiration (USG-MVA) performed

研究设计

研究类型
Interventional
主要目的
随机平行对照
盲法
未说明

入排标准

年龄范围
18 至 50(—)
性别
Female

入选标准

  • Women 18 years old or above;
  • Women with miscarriage who are suitable candidates for USG-MVA;
  • first-trimester delayed miscarriage <= 10 weeks of gestation;
  • incomplete miscarriage With POG <= 5cm;
  • hemodynamically stable;
  • tolerates well with speculum examination.

排除标准

  • Women who are not feasible for the USG-MVA;
  • cervical stenosis;
  • fibroid uterus >= 12 weeks in size;
  • known uterine malformation;
  • bleeding disorder;
  • suspicion of active infection;
  • inability to tolerate pelvic examination;
  • History of allergy to misprostol;
  • Patient refusal;
  • With history of intrauterine adhesion/ Ashermans syndrome;

研究组 & 干预措施

USG-MVA

an outpatient hysteroscopy will be performed within 6-12 weeks from their USG-MVA

traditional surgical evacuation

an outpatient hysteroscopy will be performed within 6-12 weeks from surgical evacuation procedure

结局指标

主要结局

the incidence of intrauterine adhesion

次要结局

未报告次要终点

研究者

发起方
未提供

研究点 (1)

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