Basel Postpartum Hypertension Cohort

Clinical Trial Summary

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.

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT04690660
Study type	Observational
Source	University Hospital, Basel, Switzerland
Contact	Thenral Socrates, Dr. med.
Phone	+41 61 328 6647
Email	thenral.socrates@usb.ch
Status	Recruiting
Phase
Start date	June 4, 2020
Completion date	May 2030

Basel Postpartum Hypertension Cohort — Basel-PPHT

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms