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Low-molecular-weight Heparin in Constituted Vascular Intrauterine Growth Restriction (GROWTH)

Primary Purpose

Fetal Growth Retardation

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Enoxaparin
Usual care
Sponsored by
Centre Hospitalier Universitaire de Saint Etienne
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fetal Growth Retardation focused on measuring Fetal Growth Retardation, enoxaparin

Eligibility Criteria

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

Inclusion Criteria:

  • Patient over 18 years being at a gestational age ≥ 22 and <34 weeks of gestation with vascular fetal growth retardation defined according CNGOF
  • Ultrasound Estimated fetal weight below the 10th percentile
  • Clinical and ultrasound findings suggesting pathologically impaired growth or diminished foetal well-being
  • Clinical and ultrasound findings suggesting placental insufficiency
  • Precise dating of pregnancy with an ultrasound between 11 + 0 and 13 + 6 weeks of gestation
  • Written informed consent

Exclusion Criteria:

  • multiple pregnancy or identified cause of IUGR (intra-uterine growth retardation)
  • Patient with an immediate indication of fetal extraction
  • Women with a history of venous thromboembolism or already treated with anti-coagulant
  • Women with a contraindication to enoxaparin treatment at prophylactic doses
  • Patient refusing to participate or unable to consent
  • Patient with less than 80,000 platelets / mm 3 with the initial assessment

Sites / Locations

  • Chru Brest
  • Chu Clermont-Ferrand
  • Chu Grenoble
  • Ch Lyon Sud Pierre Benite
  • HFME - Lyon Est
  • Hopital Croix Rousse Lyon
  • Ch Roanne
  • Chu Saint Etienne

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experimental group : enoxaparin

Control group

Arm Description

Experimental group will take enoxaparin (4000 Ui / Day) and will benefit from the usual care.

The control group will only benefit from the usual care.

Outcomes

Primary Outcome Measures

Number of new born with a weight inferior at the 10th percentile
With the AUDIPOG formula, the number of new born with a weight inferior at the 10th percentile will be calculated.

Secondary Outcome Measures

Change in doppler parameters of uterine arterie
Doppler parameters is a composite outcome : pulsatility index and presence of notch
Change in doppler parameters of ombilical arterie
Doppler parameters is a composite outcome : resistance index, presence of a zero diastole or reverse flow
Change in doppler fetal weight
doppler fetal weight (grams)
birth weight
birth weight (grams)
Number of new born with a weight inferior at the 3rd percentile
With the AUDIPOG formula, the number of new born with a weight inferior at the 3rd percentile will be calculated.
Number of fetal extraction
fetal extraction
number of major neonatal parameters
Major neonatal parameters is at least one or more : Perinatal death, Ischemic encephalopathy Major intra- or periventricular bleeding (grade 3 or 4), Periventricular leukomalacia, Necrotizing enterocolitis, Bronchopulmonary dysplasia or Sepsis
number of minor neonatal parameters
Minor neonatal parameters is a composite outcome : Caesarean section for fetal distress, Cord arterial pH < 7.1, Apgar score <7 at 5 minutes
Number of Major bleeding events (MB) and clinically relevant non-major bleeding events (CRNMB)
The definitions of major bleeding events and clinically major bleeding events are adapted from the ISTH definition for which were added a specific Obstetrics and Gynaecology definition Bleeding events (MB) is a composite outcome.
Number of thrombocytopenia
thrombocytopenia is a composite outcome : Thrombopenia defined by platelet count < 100 G/L Significant thrombocytopenia with HIT suspicion defined as follows:≥ 40% decline of the platelet count (compared with baseline value) occurring during the first 8 weeks following the start of HBPM Or platelet count < 80 Giga/l to terme

Full Information

First Posted
January 28, 2016
Last Updated
March 19, 2020
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
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1. Study Identification

Unique Protocol Identification Number
NCT02672566
Brief Title
Low-molecular-weight Heparin in Constituted Vascular Intrauterine Growth Restriction
Acronym
GROWTH
Official Title
Low-molecular-weight Heparin in Constituted Vascular Intrauterine Growth Restriction. Randomized Multicenter Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
July 22, 2016 (Actual)
Primary Completion Date
September 5, 2019 (Actual)
Study Completion Date
January 22, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Saint Etienne

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Intrauterine growth restriction (IUGR) is correlated to an abnormal placenta development, with an alteration of the maternal-fetal circulation, coagulation troubles, and apparition of placental infarcts. IUGR represents the third cause of perinatal mortality in France, and is associated to an important morbidity. For birth-weights < 10th percentile of the gestational age, the neonatal death risk is doubled, compared to abnormal weights. In 35% of cases, IUGR is of vascular origin and is included in the broader framework of placental vascular pathology (PVP). Up to now, studies have focused on the primary or secondary prevention of PVP. Few studies have evaluated the treatment of constituted vascular IUGR. Currently, the management of vascular IUGR is mainly based on active surveillance, or termination of pregnancy. Pathological findings suggest that placental pro-thrombotic phenomena play a role in the constitution of vascular IUGR. Since aspirin is not effective in reducing this type of event, a randomized, open-label study conducted in China compared 14-day treatment with low-molecular-weight heparin (LMWH) versus Dan-Shen (a product not used in France) after diagnosis of IUGR. This trial, including 73 patients, showed a significant improvement in average growth kinetics in the LMWH group. The mean birth weight was 2877 g in the heparin group and 2492 g in the Dan-Shen group (p <0.0001). However, no data were provided concerning the number of newborns with a birth weight <10th percentile, i.e. the risk of morbidity and mortality, or complications occurring. Due to the lack of reliable data, LMWH are not included in the currently recommended therapeutic strategy for vascular IUGR. The studies in IUGR reported to date mainly focused on primary or secondary prevention in women at risk of PVP, assessing the value of aspirin, which showed only a modest effect. No effective therapeutic strategy is available to treat patients with constituted vascular IUGR, a situation where LMWH should be more effective than antiplatelets given the vascular context.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fetal Growth Retardation
Keywords
Fetal Growth Retardation, enoxaparin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
82 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental group : enoxaparin
Arm Type
Experimental
Arm Description
Experimental group will take enoxaparin (4000 Ui / Day) and will benefit from the usual care.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
The control group will only benefit from the usual care.
Intervention Type
Drug
Intervention Name(s)
Enoxaparin
Other Intervention Name(s)
Treatment
Intervention Description
Enoxaparin will be delivered to the patients every day at the dose of 4 000 Ui.
Intervention Type
Other
Intervention Name(s)
Usual care
Other Intervention Name(s)
Classic support
Intervention Description
Patients will all benefit from the usual care
Primary Outcome Measure Information:
Title
Number of new born with a weight inferior at the 10th percentile
Description
With the AUDIPOG formula, the number of new born with a weight inferior at the 10th percentile will be calculated.
Time Frame
Week 36
Secondary Outcome Measure Information:
Title
Change in doppler parameters of uterine arterie
Description
Doppler parameters is a composite outcome : pulsatility index and presence of notch
Time Frame
baseline from delivery
Title
Change in doppler parameters of ombilical arterie
Description
Doppler parameters is a composite outcome : resistance index, presence of a zero diastole or reverse flow
Time Frame
baseline from delivery
Title
Change in doppler fetal weight
Description
doppler fetal weight (grams)
Time Frame
baseline from delivery
Title
birth weight
Description
birth weight (grams)
Time Frame
delivery
Title
Number of new born with a weight inferior at the 3rd percentile
Description
With the AUDIPOG formula, the number of new born with a weight inferior at the 3rd percentile will be calculated.
Time Frame
delivery
Title
Number of fetal extraction
Description
fetal extraction
Time Frame
before 36 weeks of gestation
Title
number of major neonatal parameters
Description
Major neonatal parameters is at least one or more : Perinatal death, Ischemic encephalopathy Major intra- or periventricular bleeding (grade 3 or 4), Periventricular leukomalacia, Necrotizing enterocolitis, Bronchopulmonary dysplasia or Sepsis
Time Frame
1 month after delivery
Title
number of minor neonatal parameters
Description
Minor neonatal parameters is a composite outcome : Caesarean section for fetal distress, Cord arterial pH < 7.1, Apgar score <7 at 5 minutes
Time Frame
1 month after delivery
Title
Number of Major bleeding events (MB) and clinically relevant non-major bleeding events (CRNMB)
Description
The definitions of major bleeding events and clinically major bleeding events are adapted from the ISTH definition for which were added a specific Obstetrics and Gynaecology definition Bleeding events (MB) is a composite outcome.
Time Frame
from randomisation to 1 month postpartum
Title
Number of thrombocytopenia
Description
thrombocytopenia is a composite outcome : Thrombopenia defined by platelet count < 100 G/L Significant thrombocytopenia with HIT suspicion defined as follows:≥ 40% decline of the platelet count (compared with baseline value) occurring during the first 8 weeks following the start of HBPM Or platelet count < 80 Giga/l to terme
Time Frame
From randomisation to 36 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient over 18 years being at a gestational age ≥ 22 and <34 weeks of gestation with vascular fetal growth retardation defined according CNGOF Ultrasound Estimated fetal weight below the 10th percentile Clinical and ultrasound findings suggesting pathologically impaired growth or diminished foetal well-being Clinical and ultrasound findings suggesting placental insufficiency Precise dating of pregnancy with an ultrasound between 11 + 0 and 13 + 6 weeks of gestation Written informed consent Exclusion Criteria: multiple pregnancy or identified cause of IUGR (intra-uterine growth retardation) Patient with an immediate indication of fetal extraction Women with a history of venous thromboembolism or already treated with anti-coagulant Women with a contraindication to enoxaparin treatment at prophylactic doses Patient refusing to participate or unable to consent Patient with less than 80,000 platelets / mm 3 with the initial assessment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tiphaine Raia-Barjat, MD
Organizational Affiliation
CHU SAINT ETIENNE
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chru Brest
City
Brest
Country
France
Facility Name
Chu Clermont-Ferrand
City
Clermont Ferrand
ZIP/Postal Code
63003
Country
France
Facility Name
Chu Grenoble
City
Grenoble
ZIP/Postal Code
38000
Country
France
Facility Name
Ch Lyon Sud Pierre Benite
City
Lyon
Country
France
Facility Name
HFME - Lyon Est
City
Lyon
Country
France
Facility Name
Hopital Croix Rousse Lyon
City
Lyon
Country
France
Facility Name
Ch Roanne
City
Roanne
Country
France
Facility Name
Chu Saint Etienne
City
St Etienne
ZIP/Postal Code
42100
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

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Low-molecular-weight Heparin in Constituted Vascular Intrauterine Growth Restriction

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