Changes in Central Arterial Pressure of Normotensive Women Taking Nifedipine for Tocolysis

NCT02902354 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2017-11-13

No results posted yet for this study

Summary

To determine the central blood pressure changes in normotensive women who are receiving nifedipine for uterine contraction suppression

Conditions

  • Tocolysis With Nifedipine

Interventions

OTHER

Nifedipine for tocolysis

observational

Sponsors & Collaborators

  • St. Louis University

    lead OTHER

Principal Investigators

  • Jennifer Goldkamp, MD · St. Louis University

Study Design

Allocation
NA
Purpose
SCREENING
Masking
NONE
Model
SINGLE_GROUP

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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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 NCT02902354 on ClinicalTrials.gov