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Completed

NCT Number: NCT01390051

Can Low Molecular Weight Heparin During Pregnancy With Intrauterine Growth Restriction Increase Birth Weight?

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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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

Consultant phD professor Anne-Mette Hvas, Aarhus, Central Jutland, Denmark

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About this study

Clinical purpose:

  • To examine whether treatment with low molecular weight heparin in pregnant women with Intrauterine Growth Restriction (IUGR)increases the birth weight of the child. Our hypothesis is that an increased birth weight leads to reduced morbidity and mortality among these children.

Laboratory purposes:

  • To evaluate three new methods to monitor the effect of LMWH.
  • To investigate if 2 biochemical markers are positive predictors of IUGR IUGR is defined as a foetus that grows less than expected. IUGR is estimated to occur in up to 5% of all pregnancies, and IUGR is the second most common cause of perinatal morbidity and mortality. Thus, 75% of all stillbirths are caused by IUGR. IUGR is diagnosed by ultrasonography. In IUGR the uteroplacental blood flow is often compromised resulting in foetal growth restriction.

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Singleton pregnancy
  • IUGR shown by ultrasonography:
  • Can understand and read Danish

Exclusion criteria

  • Age below 18 years
  • Pregestational weight < 90 kilograms
  • Not able to give informed consent
  • Chronic kidney disease with creatinine >150 μmol/l
  • Chronic hypertension with blood pressure >140/90 mmHg
  • Diabetes mellitus; type 1 or 2 or gestational diabetes
  • Inflammatory bowel disease
  • Severe heart disease (including mechanical heart valves)
  • Drug or alcohol abuse
  • Known coagulopathy (von Willebrand disease, thrombocytopenia, carrier of haemophilia)
  • Treatment with vitamin K antagonists
  • Known allergy to low LMWH
  • Previous heparin-induced thrombocytopenia (HIT (type II))
  • Clinically significant bleeding within the last month
  • Women with indication for prophylactic treatment with LMWH during pregnancy e.g. previous thromboembolic disease or serious types of thrombophilia (deficiency of antithrombin, protein C or protein S)
  • Chromosome anomaly in the child
  • Severe malformations in the child
  • Contraindication to Innohep®
  • Gestational week > 32 weeks

Treatment and study plan

Innohep (Tinzaparin)

Drug

Dose: 4,500 IU daily in half of the study populationrandomised to treatment

Other names: Innohep

tinzaparin

Drug

Dose 4,500 IE daily

Other names: Innohep

Primary outcomes

  1. birth weight

    Time frame: Birth weight registered at birth

    We compare birth weight in children born of women from the 2 study arms

Secondary outcomes

  1. maternal morbidity

    Time frame: Comorbidity registered up to one year after birth

Sponsors and collaborators

Lead sponsor

University of Aarhus

Other

Collaborators

  • Aarhus University Hospital
  • LEO Pharma

Registry information

Official study title

Can Treatment With Low Molecular Weight Heparin During Pregnancy With Intrauterine Growth Restriction Increase Birth Weight?

Acronym: IUGR

Important dates

Study start
2011
Primary completion
2016
Study completion
2016
First posted
Jul 8, 2011
Registry last updated
Aug 18, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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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