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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 weeks3 visits
Treatment ~ Varies
Follow Up ~ between enrollment and delivery, assessed up to 18 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~between enrollment and delivery, assessed up to 18 weeks
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 moreTrial 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
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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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