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NCT00641784

A Randomized Trial of Oral Nifedipine Versus Intravenous Magnesium Sulfate in the Acute Management of Preterm Labor in Women With Singleton Gestations, Intact Fetal Membranes, and Positive Vaginal Fetal Fibronectin

Terminated Phase 3 Last updated 17 September 2009
What this trial tests

Phase 3 trial testing Magnesium in Labor, Premature in 200 participants. Terminated before completion.

Timeline
1 March 2008
Primary endpoint
1 March 2012
1 March 2012

Quick facts

Lead sponsorMemorialCare
PhasePhase 3
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment200
Start date1 March 2008
Primary completion1 March 2012
Estimated completion1 March 2012
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

MemorialCare — full company profile →

Who can join

Adults 18 to 55, female only, with Labor, Premature. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

In women with singleton gestations, to contemporarily assess the efficacy of oral nifedipine versus intravenous magnesium sulfate in the acute management of preterm labor in terms of defined early and late neonatal measures

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Tocolytics for delaying preterm birth: a network meta-analysis (0924).
    Wilson A, Hodgetts-Morton VA, Marson EJ, Markland AD, et al · · 2022 · cited 37× · PMID 35947046 · DOI 10.1002/14651858.cd014978.pub2

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing