Changes in Central Arterial Pressure When Comparing Nifedipine/Labetalol for Routine Hypertension Control in Pregnancy

NCT02912910 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2017-11-13

No results posted yet for this study

Summary

To study central blood pressure changes caused by commonly used high blood pressure medications in pregnancy.

Conditions

Interventions

OTHER

Nifedipine

patients will be assigned to antihypertensive medications by their physicians in the course of their routine care

OTHER

Labetalol

patients will be assigned to antihypertensive medications by their physicians in the course of their routine care

Sponsors & Collaborators

  • St. Louis University

    lead OTHER

Principal Investigators

  • Jennifer Goldkamp · St. Louis University

Eligibility

Min Age
14 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2017-01-31
Completion
2017-01-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02912910 on ClinicalTrials.gov