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临床试验/PACTR201804003324963
PACTR201804003324963已完成未知

Immediate Versus Delayed Insertion of the Copper IUD After Second-trimester Medical Abortion - a Randomised Controlled Trial.

niversity of Cape Town Faculty of Health Sciences0 个研究点目标入组 110 人开始时间: 2018年4月12日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
110

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
18 Year(s) 至 60 Year(s)(—)
性别
Male

入选标准

  • Age 18 years or older;
  • Able to speak English, Afrikaans or Xhosa;
  • Requesting abortion and eligible for legal termination of pregnancy according to standard practice at the hospital;
  • Gestational age (GA) 13-20 weeks verified by ultrasound (most women will be >16 weeks GA at the study site, however women with GA 13-15 weeks will be eligible);
  • Interested and eligible for the copper IUD as a post-abortion contraceptive method;
  • Willing to do a telephone interview at 3- and 6-months post-abortion;
  • Able to provide a working phone telephone number to allow for contact for follow up interviews;
  • Willing to be randomized to immediate or delayed IUD insertion; and
  • Willing and able to provide informed consent

排除标准

  • Active pelvic inflammatory disease, pelvic tuberculosis; severe thrombocytopenia;
  • Severe dysmenorrhea
  • Copper allergy
  • Hb <10g/dL
  • Uterine anomaly preventing placement of the IUD; cervical cancer or carcinoma in-situ, untreated high grade squamous intraepithelial lesions
  • Desire for repeat pregnancy in following 12 months
  • Hemorrhage; or ruptured uterus

研究者

发起方
niversity of Cape Town Faculty of Health Sciences

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