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Completed

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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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Karma Medical Clinic, Kitchener, Ontario, Canada

Loading trial locations.

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

Progesterone

Drug

Placebo

Drug

Primary outcomes

  1. Miscarriage

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

    Occurrence of a miscarriage (<20 weeks)

  2. Preterm birth

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

    Occurrence of preterm birth (<37 weeks)

Secondary outcomes

  1. Maternal outcomes

    Time frame: From 6-8 weeks of pregnancy until 6 weeks post delivery

    Antenatal admissions, treatment of preterm labor etc.

  2. Neonatal outcomes

    Time frame: 2 days to 6 weeks post delivery

    Malformations, growth restriction, prematurity associated morbidity, etc.

  3. 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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