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
About this trial
This is an interventional treatment trial for Fetal Growth Retardation focused on measuring birth weight, thrombosis, anticoagulant therapy
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
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
NCT ID
NCT01390051
First Posted
July 6, 2011
Last Updated
August 17, 2016
Sponsor
University of Aarhus
Collaborators
Aarhus University Hospital, LEO Pharma
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
Learn more about this trial
Can Low Molecular Weight Heparin During Pregnancy With Intrauterine Growth Restriction Increase Birth Weight?
We'll reach out to this number within 24 hrs