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临床试验/NCT01734434
NCT01734434已完成不适用

A Multicenter, Observational Study to Identify Factors That Influence Access of Pregnant Women and Their Infants to Their Local Healthcare Systems

Novartis Vaccines10 个研究点 分布在 4 个国家目标入组 3,243 人开始时间: 2012年11月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
3,243
试验地点
10
主要终点
Percentage of Subjects Delivering at a Non-study Site.

研究概览

简要总结

This study collected information regarding the factors that might influence access of pregnant women to the local healthcare system. The main visits of the study screened & enrollment, delivery and 90 day infant follow-up. Data were collected mainly from questionnaires administered to pregnant women at these visits. The questionnaires contained the following standard questions which were asked at each visit, in addition to some visit-specific questions related to delivery and health status of infants up to 90 days of age. The standard questions related to the following aspects:

  • Logistics of transportation to the study site (type, time it takes, cost incurred)
  • Accessibility to a telephone/cell phone
  • Provisions of alternative child care during site visits if there are other children under the subject's care

研究设计

研究类型
Observational
观察模型
Ecologic Or Community
时间视角
Prospective

入排标准

性别
Female
接受健康志愿者

入选标准

  • Pregnant women with gestational age of greater than or equal to 24 weeks at the time of enrollment
  • Subject / subject's parents or a legal representative who has given written consent after the nature of the study has been explained according to local regulatory requirements
  • Pregnant women of gestational age between 28 weeks and 34 weeks 6/7 days

排除标准

  • 未提供

结局指标

主要结局

Percentage of Subjects Delivering at a Non-study Site.

时间窗: Baseline until average of 24 weeks

The percentage of subjects who delivered at a non-study site relative to the number of enrolled subjects was calculated.

Percentage of Subjects Delivering at a Study Site.

时间窗: Baseline until average of 24 weeks

The percentage of subjects who delivered at the study site relative to the number of enrolled subjects was calculated

次要结局

  • Number of Infants Brought to Study Site During Infant Follow up (90 Days Post-delivery)(Delivery to Day 90 post-delivery (Infant follow-up))
  • Number of Infants Born Live, Reported Sick and Brought to a Study or Non-study Health Care Facility Site.(Delivery to Day 90 post-delivery (Infant follow-up))

研究者

发起方
Novartis Vaccines
申办方类型
Industry
责任方
Sponsor

研究点 (10)

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