ISRCTN11042045
Active, not recruiting
未知
Randomised controlled trial of self-management of postnatal antihypertensive treatment
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Monitoring of hypertension in women following hypertensive pregnancy
- Sponsor
- niversity of Oxford
- Enrollment
- 628
- Status
- Active, not recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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
Outcomes
Primary Outcomes
Not specified
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