Clinical Research Directory

Browse clinical research sites, groups, and studies.

1 clinical study listed.

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Superimposed Pre-Eclampsia

Tundra lists 1 Superimposed Pre-Eclampsia clinical trial. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT06785116

A Randomized, Placebo-controlled Trial of DAPAgliflozin (DAPA) for Cardiovascular Risk Reduction in the Postpartum Period of Hypertensive Pregnancies (HP)

This trial is a pilot-scale, single institution randomized, placebo-controlled trial to assess the feasibility, acceptability, and efficacy of administering dapagliflozin for cardiovascular risk reduction in the postpartum period. The target population is patients at high risk of adverse cardiovascular outcomes within five years post-delivery. Eligible participants will be randomized to receive either: 1) dapagliflozin (10mg daily) for six months (DAPA group) or 2) an orally administered, daily placebo (Control group). The study hypothesizes: The dapagliflozin group will have higher cardiovascular risk reduction scores than the Control Group.

Gender: FEMALE

Ages: 18 Years - Any

Updated: 2026-03-04

1 state

Gestational Hypertension

Hypertension in Pregnancy

Pre-Eclampsia