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Clinical Trials/ISRCTN11042045
ISRCTN11042045
Active, not recruiting
未知

Randomised controlled trial of self-management of postnatal antihypertensive treatment

niversity of Oxford0 sites628 target enrollmentJune 11, 2024

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.

Registry
who.int
Start Date
June 11, 2024
End Date
December 1, 2026
Last Updated
last year
Study Type
Interventional
Sex
Female

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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