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UnknownNCT01985594

Utrogestan Versus Nifedipine as Tocolysis for Preterm Labor: a Randomised Controlled Trial

STUDY ON EFFICACY OF UTROGESTAN AS TOCOLYSIS FOR PRETERM LABOR

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
32 (estimated)
Sponsor
nor zila hassan malek · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

RESEARCH HYPOTHESIS -Incidence of preterm delivery is lower in women treated with oral micronized progesterone (Utrogestan) as acute tocolysis agent compare to Nifedipine group with fewer maternal side effect

Conditions

Interventions

TypeNameDescription
DRUGutrogestanOral Tablet Utrogestan 400 mg daily for 2 days
DRUGNifedipineTablet Nifedipine 20 mg stat then 20 mg after 30 minutes if contraction persist and another 20mg after 30 minutes if contraction still persist followed by 10 mg three times daily for 2 days

Timeline

Start date
2013-11-01
Primary completion
2014-07-01
Completion
2014-10-01
First posted
2013-11-15
Last updated
2013-11-15

Locations

1 site across 1 country: Malaysia

Source: ClinicalTrials.gov record NCT01985594. Inclusion in this directory is not an endorsement.

Utrogestan Versus Nifedipine as Tocolysis for Preterm Labor: a Randomised Controlled Trial (NCT01985594) · Clinical Trials Directory