...
首页> 外文期刊>Trials >Immediate vs. delayed insertion of intrauterine contraception after second trimester abortion: study protocol for a randomized controlled trial
【24h】

Immediate vs. delayed insertion of intrauterine contraception after second trimester abortion: study protocol for a randomized controlled trial

机译:妊娠中期流产后立即插入宫内避孕药与延迟插入宫内避孕药:一项随机对照试验的研究方案

获取原文
           

摘要

Background We describe the rationale and protocol for a randomized controlled trial (RCT) to assess whether intrauterine contraception placed immediately after a second trimester abortion will result in fewer pregnancies than current recommended practice of intended placement at 4 weeks post-abortion. Decision analysis suggests the novel strategy could substantially reduce subsequent unintended pregnancies and abortions. This paper highlights considerations of design, implementation and evaluation of a trial expected to provide rigorous evidence for appropriate insertion timing and health economics of intrauterine contraception after second trimester abortion. Methods/Design Consenting women choosing to use intrauterine contraception after abortion for a pregnancy of 12 to 24 weeks will be randomized to insertion timing groups either immediately (experimental intervention) or four weeks (recommended care) post abortion. Primary outcome measure is pregnancy rate at one year. Secondary outcomes include: cumulative pregnancy rates over five year follow-up period, comprehensive health economic analyses comparing immediate and delayed insertion groups, and device retention rates, complication rates (infection, expulsion) and, contraceptive method satisfaction. Web-based Contraception Satisfaction Questionnaires, clinical records and British Columbia linked health databases will be used to assess primary and secondary outcomes. Enrolment at all clinics in the province performing second trimester abortions began in May 2010 and is expected to complete in late 2011. Data on one year outcomes will be available for analysis in 2014. Discussion The RCT design combined with access to clinical records at all provincial abortion clinics, and to information in provincial single-payer linked administrative health databases, birth registry and hospital records, offers a unique opportunity to evaluate such an approach by determining pregnancy rate at one through five years among enrolled women. We highlight considerations of design, implementation and evaluation of a trial expected to provide rigorous evidence for appropriate insertion timing and health economics of intrauterine contraception after second trimester abortion. Trial registration Current Controlled Trials ISRCTN19506752
机译:背景我们描述了一项随机对照试验(RCT)的基本原理和方案,以评估在流产后4个月流产后立即放置宫内避孕是否会比目前建议的预定放置做法少怀孕。决策分析表明,这种新策略可以大大减少随后的意外怀孕和流产。本文重点介绍了一项设计,实施和评估试验的考虑,该试验有望为孕中期流产后子宫内避孕的适当插入时机和健康经济性提供严格的证据。方法/设计同意在流产后选择使用宫内避孕的妇女怀孕12至24周,将被随机分配到流产后立即(实验干预)或四个星期(建议的护理)的插入时间组。主要结局指标是一年的妊娠率。次要结果包括:五年随访期内的累计妊娠率,比较即刻和延迟插入组的综合健康经济分析,器械保留率,并发症发生率(感染,驱逐)和避孕方法的满意度。基于网络的避孕满意度问卷,临床记录和不列颠哥伦比亚省链接的健康数据库将用于评估主要和次要结局。该省所有进行中期流产的诊所的入组于2010年5月开始,预计于2011年底完成。有关一年结局的数据将在2014年进行分析。讨论RCT设计结合所有省份的临床记录访问人工流产诊所,以及省级单付款人链接的行政健康数据库,出生登记和医院记录中的信息,提供了一个独特的机会来评估这种方法,方法是确定已登记妇女中一到五年的怀孕率。我们着重于设计,实施和评估试验的考虑因素,该试验有望为孕中期流产后子宫内避孕的适当插入时机和健康经济性提供严格的证据。试用注册电流对照试验ISRCTN19506752

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号