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临床试验/ACTRN12614000773639
ACTRN12614000773639终止未知

Trio Analysis using Whole Genome Sequencing to Assist Interpretation of Autopsy Findings for Families who have Experienced a Perinatal Death Without any Definitive Cause

Mater Health Services0 个研究点目标入组 300 人开始时间: 2014年7月21日最近更新:

试验速览

阶段
未知
状态
终止
发起方
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
Hours 至 28 Days(—)
性别
All

入选标准

  • Criteria for Inclusion – Perinatal Cases:
  • 1.Perinatal death occurring at Mater Mother’s Hospital between 2010 and 2014;
  • 2.After attempting to contact both parents, minimally one parent has been contacted after 3 attempts and is willing to participant in this clinical trial
  • Criteria for Inclusion – Biological Parent Participants:
  • 1.A baby (from 20 weeks gestation to 28 days postpartum) who passed away at Mater Mother’s Hospital between 2010 to 2014
  • 2.Able to attend at least the initial study visit for informed consent and blood collection
  • 3.Important medical information pertaining to the deceased infant is part of the mother’s medical notes

排除标准

  • Criteria for Exclusion – Perinatal Cases:
  • 1.Coronial Case
  • 2.Insufficient or inadequate DNA sample
  • 3.Only the father is contactable and critical medical information about the deceased infant resides in the mother’s medical notes.
  • 4.One parent refuses permission for their child’s DNA to be used for the study.
  • Criteria for Exclusion – Biological Parent Participants:
  • 1.A baby (from 20 weeks gestation to 28 days postpartum) who passed away at Mother Mother’s Hospital between 2010 and 2014 that was/is the subject of a coronial investigation
  • 2.A concurrent condition that may limit the decision-making capabilities of the participant during the informed consent process
  • 3.Blood Donation of >450ml within 30 days of the initial study visit

研究者

发起方
Mater Health Services

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