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Swiss Postpartum Hypertension Cohort

Recruitingn/aAges 18 Years - anyFemaleUniversity Hospital, Basel, Switzerland
NCT04690660 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This open label, prospective observational, single-center registry is to study short-, intermediate-and long-term course of postpartum hypertension and predictors/risk factors associated with long term cardiovascular and renal risk. Current disease management strategies will be evaluated.

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📋 Eligibility rules (as published)
Inclusion Criteria: * all women with hypertensive disorders of pregnancy * postpartum hypertension (blood pressure measurements of systolic ≥140 and/or diastolic ≥ 90mmHg or antihypertensive therapy within the first 14 days after delivery) * women with preexisting hypertension or * women on antihypertensive medication Exclusion Criteria: * delivery \> 14 days * lack of consent to participate in the study, language barriers or lack of general understanding
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What it tests

  • Data collection for parameters of organ damage (cardiac and renal blood markers)
  • Data collection for blood pressure (BP)
  • Home-based blood pressure management (substudy)
  • Biomarker Profiles (substudy)
  • Data collection on patient reported outcomes
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Where

1 site
Medical Outpatient Department and Hypertension Clinic, University Hospital Basel
Basel, Switzerland
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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