Innohep (Tinzaparin)
DrugDose: 4,500 IU daily in half of the study populationrandomised to treatment
Other names: Innohep
NCT Number: NCT01390051
The purpose of the study is to investigate if treatment with an anticoagulant drug increases birth weight in pregnancies complicated by fetal growth restriction.
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Notify Me18 year and older
Female
Interventional
Phase 4
Consultant phD professor Anne-Mette Hvas, Aarhus, Central Jutland, Denmark
Clinical purpose:
Laboratory purposes:
Design: The study is a prospective randomised study where pregnant women with suspected severe IUGR are randomised either to treatment with Innohep® or no treatment. Half of the women receive Innohep® and half of the women do not receive treatment.
Endpoints The primary endpoint is the difference in birth weight in children born of women receiving Innohep® during pregnancy and children born of women who have not received Innohep® during pregnancy
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Dose: 4,500 IU daily in half of the study populationrandomised to treatment
Other names: Innohep
Dose 4,500 IE daily
Other names: Innohep
Time frame: Birth weight registered at birth
We compare birth weight in children born of women from the 2 study arms
Time frame: Comorbidity registered up to one year after birth
University of Aarhus
Other
Can Treatment With Low Molecular Weight Heparin During Pregnancy With Intrauterine Growth Restriction Increase Birth Weight?
Acronym: IUGR
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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