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临床试验/NCT01223521
NCT01223521已完成不适用

Systematic Provision of Intrauterine Contraception After First Trimester Abortion - Effects on Quality of Life and Risk of Repeat Abortion. A Randomized, Prospective Trial.

Helsinki University Central Hospital2 个研究点 分布在 1 个国家目标入组 748 人开始时间: 2010年9月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
748
试验地点
2
主要终点
Number of repeat abortions

研究概览

简要总结

A randomized prospective study on the effects of immediate provision of intrauterine contraception after first trimester induced abortion - effects on repeat abortions and quality of life.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Duration of pregnancy < 12 weeks.
  • Age ≥18 years

排除标准

  • Contraindication for spiral insertion: uterine anomaly, infection, copper allergy (Cu-IUD).

研究组 & 干预措施

Immediate intrauterine contraception

Experimental

IUD (either Cu-IUD or LNG-IUS) inserted immediately after abortion.

干预措施: Immediate intrauterine contraception (Device)

Control group

No Intervention

Post-abortal contraception is prescribed by the hospital but on the responsibility of the patient.

结局指标

主要结局

Number of repeat abortions

时间窗: 5 years

Number of subsequent abortions during five years follow-up time.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Elina Pohjoranta

MD

Helsinki University Central Hospital

研究点 (2)

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