NCT Number: NCT02145767
Progesterone for the Prevention of Miscarriage and Preterm Birth in Women With First Trimester Bleeding: PREEMPT Trial
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.
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Notify MeKey information
Conditions
Age range
18 year–45 year
Sex eligibility
Female
Study type
Interventional
Phase
Phase 2
Primary location
Karma Medical Clinic, Kitchener, Ontario, Canada
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
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
Treatment and study plan
Placebo
DrugPrimary 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
Time frame: From 6-8 weeks of pregnancy until 6 weeks post delivery
Antenatal admissions, treatment of preterm labor etc.
-
Neonatal outcomes
Time frame: 2 days to 6 weeks post delivery
Malformations, growth restriction, prematurity associated morbidity, etc.
-
Healthcare outcomes
Time frame: From 6-8 weeks of pregnancy until 6 weeks post delivery
Hospital costs, etc
Sponsors and collaborators
Lead sponsor
Sir Mortimer B. Davis - Jewish General Hospital
Other
Collaborators
- Canadian Institutes of Health Research (CIHR)
Registry information
Important dates
- Study start
- 2014
- Primary completion
- 2021
- Study completion
- 2021
- First posted
- May 23, 2014
- Registry last updated
- Aug 23, 2021
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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