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