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Calcium Channel Blocker

Nifedipine 30MG for Pre-eclampsia

Phase 4
Waitlist Available
Research Sponsored by Ohio State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at delivery
Awards & highlights

Study Summary

This trial is testing whether or not Nifedipine can help with preeclampsia when labor is induced.

Eligible Conditions
  • Pre-eclampsia

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~between enrollment and delivery, assessed up to 18 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and between enrollment and delivery, assessed up to 18 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Number of Participants With the Change in Blood Pressure (Both Systolic and Diastolic) Under the Treatment of NIfedipine 30mg XL Versus Placebo
Secondary outcome measures
Number of Participants Stratified by Route of Delivery
Number of Participants Who Required Acute Antihypertension Treatments Postpartum
Number of Participants With Hypotension of ≥30% Decrease in Blood Pressure From Baseline Following Acute Antihypertensive Therapy
+1 more

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Nifedipine 30MGActive Control1 Intervention
Oral administration of 30mg Nifedipine XL q24 hours until delivery
Group II: PlaceboPlacebo Group1 Intervention
Matching placebo group q24hrs until delivery

Find a Location

Who is running the clinical trial?

Ohio State UniversityLead Sponsor
826 Previous Clinical Trials
502,575 Total Patients Enrolled

Frequently Asked Questions

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~23 spots leftby Apr 2025