Labetalol or Nifedipine for Control of Postpartum Hypertension: A Randomized Controlled Trial

Description

Randomized trial comparing risk of hospital readmission and hypertensive complications between patients managed on Labetalol compared to Nifedipine.

Conditions

Postpartum Preeclampsia, Hypertension in Pregnancy

Study Overview

Study Details

Study overview

Randomized trial comparing risk of hospital readmission and hypertensive complications between patients managed on Labetalol compared to Nifedipine.

Labetalol or Nifedipine for Control of Postpartum Hypertension: A Randomized Controlled Trial

Labetalol or Nifedipine for Control of Postpartum Hypertension: A Randomized Controlled Trial

Condition
Postpartum Preeclampsia
Intervention / Treatment

-

Contacts and Locations

Omaha

Nebraska Methodist Women's Hospital, Omaha, Nebraska, United States, 68022

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Contraindication to either Nifedipine or Labetalol
  • * HR \<60 or \>110
  • * Native language other than English or Spanish

Ages Eligible for Study

19 Years to

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Nebraska Methodist Health System,

Todd Lovgren, MD, PRINCIPAL_INVESTIGATOR, Nebraska Methodist Health System

Study Record Dates

2024-12-01