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临床试验/NCT01713153
NCT01713153已完成不适用

Preventing Postpartum Hemorrhage: Examining Two Strategies for PPH Prevention in Communities: Misoprostol and Oxytocin Uniject in Senegal

Gynuity Health Projects1 个研究点 分布在 1 个国家目标入组 1,365 人开始时间: 2012年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,365
试验地点
1
主要终点
Mean change in hemoglobin

研究概览

简要总结

This is a large, community-based, cluster-randomized trial to compare routine prophylactic use of 600 mcg oral misoprostol and 10 IU oxytocin delivered by UnijectTM intramuscularly during the third stage of labor

详细描述

This study will assess the programmatic implications (including feasibility, acceptability, risks and benefits) at the community level of the introduction of misoprostol and/or oxytocin in UnijectTM for the prevention of PPH and will help to identify the appropriate niche for both drugs.

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
None

入排标准

性别
Female
接受健康志愿者

入选标准

  • women delivering in community health centers (case de sante) with a trained study provider (matrone) who are able to provide informed consent

排除标准

  • women with known contraindications to prostaglandins

研究组 & 干预措施

Misoprostol

Experimental

600 mcg oral misoprostol administered during the third stage of labor

干预措施: Misoprostol (Drug)

UnijectTM

Experimental

10 IU oxytocin delivered IM with UnijectTM during he third stage of labor

干预措施: UnijectTM (Device)

结局指标

主要结局

Mean change in hemoglobin

时间窗: during 3rd trimester and 1-3 days postpartum

To establish the comparable effectiveness of two technologies, individual pre- and post-delivery Hb measures will be taken to calculate change in Hb. This will be done using a Hemocue Hemoglobin machine + cuvette (HemoCue, Angelholm, Sweden). The Hemocue is a simple means of collecting Hb measures at the community-level where traditional laboratory techniques are not feasible

次要结局

  • change in hemoglobin ≥ 2 g/dL(during third trimester and 1-3 days postpartum)
  • Occurrence and management of side effects(1 hour postpartum)
  • correct timing of drug administration(collected immediately following birth, verified 1-3 days postpartum)
  • additional interventions(during birth)
  • referrals(0-3 days postpartum)
  • acceptability(1-3 days postpartum)

研究者

发起方
Gynuity Health Projects
申办方类型
Other
责任方
Sponsor

研究点 (1)

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