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临床试验/ISRCTN11042045
ISRCTN11042045进行中(未招募)Unknown

Randomised controlled trial of self-management of postnatal antihypertensive treatment

niversity of Oxford0 个研究点目标入组 628 人开始时间: 2024年6月11日最近更新:
适应症

试验速览

阶段
Unknown
状态
进行中(未招募)
入组人数
628

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

性别
Female

入选标准

  • 1. Participant is willing and able to give informed consent for participation in the study
  • 2. People who have recently given birth within the last 7 days
  • 3. Aged 18 years or above
  • 4. Participant with pregnancy hypertension including: chronic/essential hypertension (predating current pregnancy or requiring treatment before 20/40), or gestational hypertension (new-onset hypertension from 20/40 of index pregnancy) or pre-eclampsia (hypertension (GH or with proteinuria or metabolic changes), prior to their discharge from hospital post-delivery.
  • 5. Participant still requiring antihypertensive medication at randomisation following delivery
  • 6. Able and willing to comply with trial requirements
  • 7. Willing to allow their primary and secondary healthcare teams, if appropriate, to be notified of participation in the trial
  • 8. Access to a smartphone compatible with the app

排除标准

  • 1. Participant does not wish to self-monitor/self-manage their blood pressure
  • 2. Participant already taking part in another trial that might affect their anti-hypertensive prescription

研究者

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