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

Primary Purpose

Fetal Growth Retardation

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Innohep (Tinzaparin)
tinzaparin
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fetal Growth Retardation focused on measuring birth weight, thrombosis, anticoagulant therapy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Singleton pregnancy
  2. IUGR shown by ultrasonography:
  3. Can understand and read Danish

Exclusion Criteria:

  1. Age below 18 years
  2. Pregestational weight < 90 kilograms
  3. Not able to give informed consent
  4. Chronic kidney disease with creatinine >150 μmol/l
  5. Chronic hypertension with blood pressure >140/90 mmHg
  6. Diabetes mellitus; type 1 or 2 or gestational diabetes
  7. Inflammatory bowel disease
  8. Severe heart disease (including mechanical heart valves)
  9. Drug or alcohol abuse
  10. Known coagulopathy (von Willebrand disease, thrombocytopenia, carrier of haemophilia)
  11. Treatment with vitamin K antagonists
  12. Known allergy to low LMWH
  13. Previous heparin-induced thrombocytopenia (HIT (type II))
  14. Clinically significant bleeding within the last month
  15. 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)
  16. Chromosome anomaly in the child
  17. Severe malformations in the child
  18. Contraindication to Innohep®
  19. Gestational week > 32 weeks

Sites / Locations

  • Consultant phD professor Anne-Mette Hvas
  • Department of Obstetrics
  • Department of Obstetrics

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Innohep

no treatment

Arm Description

Tinzaparin 4500 I.U. sub cutaneous once daily until gestational week 37

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

maternal morbidity

Full Information

First Posted
July 6, 2011
Last Updated
August 17, 2016
Sponsor
University of Aarhus
Collaborators
Aarhus University Hospital, LEO Pharma
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1. Study Identification

Unique Protocol Identification Number
NCT01390051
Brief Title
Can Low Molecular Weight Heparin During Pregnancy With Intrauterine Growth Restriction Increase Birth Weight?
Acronym
IUGR
Official Title
Can Treatment With Low Molecular Weight Heparin During Pregnancy With Intrauterine Growth Restriction Increase Birth Weight?
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
July 2016 (Actual)
Study Completion Date
July 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
Collaborators
Aarhus University Hospital, LEO Pharma

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to investigate if treatment with an anticoagulant drug increases birth weight in pregnancies complicated by fetal growth restriction.
Detailed Description
Clinical purpose: 1. 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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fetal Growth Retardation
Keywords
birth weight, thrombosis, anticoagulant therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Innohep
Arm Type
Active Comparator
Arm Description
Tinzaparin 4500 I.U. sub cutaneous once daily until gestational week 37
Arm Title
no treatment
Arm Type
No Intervention
Intervention Type
Drug
Intervention Name(s)
Innohep (Tinzaparin)
Other Intervention Name(s)
Innohep
Intervention Description
Dose: 4,500 IU daily in half of the study populationrandomised to treatment
Intervention Type
Drug
Intervention Name(s)
tinzaparin
Other Intervention Name(s)
Innohep
Intervention Description
Dose 4,500 IE daily
Primary Outcome Measure Information:
Title
birth weight
Description
We compare birth weight in children born of women from the 2 study arms
Time Frame
Birth weight registered at birth
Secondary Outcome Measure Information:
Title
maternal morbidity
Time Frame
Comorbidity registered up to one year after birth

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne-Mette Hvas, PhD, professor
Organizational Affiliation
Department of Clinical Biochemistry, Aarhus University Hospital, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Consultant phD professor Anne-Mette Hvas
City
Aarhus
State/Province
Central Denmark Region
ZIP/Postal Code
8200
Country
Denmark
Facility Name
Department of Obstetrics
City
Herning
ZIP/Postal Code
7400
Country
Denmark
Facility Name
Department of Obstetrics
City
Randers
Country
Denmark

12. IPD Sharing Statement

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

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