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Clinical Trials/NCT02145767
NCT02145767
Completed
Phase 2

Progesterone for the Prevention of Miscarriage and Preterm Birth in Women With First Trimester Bleeding: PREEMPT Trial

Sir Mortimer B. Davis - Jewish General Hospital7 sites in 1 country850 target enrollmentDecember 2014

Overview

Phase
Phase 2
Intervention
Progesterone
Conditions
Miscarriage
Sponsor
Sir Mortimer B. Davis - Jewish General Hospital
Enrollment
850
Locations
7
Primary Endpoint
Miscarriage
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Miscarriages and preterm births are common and serious events affecting women, families, and healthcare systems on many levels. One of the risk factors for miscarriage and preterm birth is bleeding in the first trimester of pregnancy. Progesterone, a hormone that plays a key role during pregnancy, has been proposed as a possible medication to be used in pregnancy to prevent miscarriage and preterm birth among women who have bleeding in their first trimester of pregnancy. Unfortunately, unless sound clinical evidence is obtained through a clinical trial, whether or not progesterone can indeed prevent miscarriage and preterm birth remains uncertain and thus is not a recommended treatment in women with early pregnancy bleeding. The purpose of our study is to evaluate the effect of progesterone for the prevention of miscarriage and preterm birth among women with early pregnancy bleeding. We will carry out a clinical trial in which 850 women will be randomized to receive either progesterone supplementation (425 women) or a similarly appearing placebo (425 women) and the outcome of their pregnancy will be compared.

Registry
clinicaltrials.gov
Start Date
December 2014
End Date
February 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Sir Mortimer B. Davis - Jewish General Hospital
Responsible Party
Principal Investigator
Principal Investigator

Haim Abenhaim

Obstetrician & Gynecologist, Maternal Fetal Medicine Specialist, Director of Perinatal Research

Sir Mortimer B. Davis - Jewish General Hospital

Eligibility Criteria

Inclusion Criteria

  • Live intrauterine singleton pregnancy of \<14 weeks by crown-rump length on ultrasound with documented fetal cardiac activity
  • Presence of a perigestational (subchorionic) hemorrhage on ultrasound

Exclusion Criteria

  • Contraindication to Progesterone
  • Any indication for progesterone

Arms & Interventions

Progesterone

Progesterone 200mg suppository administered vaginally at bedtime until 34 completed weeks of pregnancy.

Intervention: Progesterone

Placebo

Similar appearing suppository containing vehicle alone administered vaginally at bedtime until 34 completed weeks of pregnancy.

Intervention: Placebo

Outcomes

Primary Outcomes

Miscarriage

Time Frame: From 6-8 weeks of pregnancy until miscarriage

Occurrence of a miscarriage (\<20 weeks)

Preterm birth

Time Frame: From 6-8 weeks of pregnancy until delivery

Occurrence of preterm birth (\<37 weeks)

Secondary Outcomes

  • Maternal outcomes(From 6-8 weeks of pregnancy until 6 weeks post delivery)
  • Neonatal outcomes(2 days to 6 weeks post delivery)
  • Healthcare outcomes(From 6-8 weeks of pregnancy until 6 weeks post delivery)

Study Sites (7)

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