MorbiMortality Amelioration in Preeclamptic Primiparas Study. MoMA Pre Prim Study (MOMA)
Primary Purpose
Pregnancy, Primiparity, Hypertension
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Transmission of sFlt-1 results to the investigator
No transmission of the sFlt-1 results to the investigator
Sponsored by
About this trial
This is an interventional prevention trial for Pregnancy focused on measuring Preeclampsia, Hypertension, Intra uterine growth retardation, Antiangiogenic factor, Prevention
Eligibility Criteria
Inclusion Criteria:
- Pregnant womenAge ≥ 18 years
- Followed in our center before the 28th week of gestation
- Under social security coverage
- Signed informed consent
Exclusion Criteria:
- Age < 18 years
- Followed in our center after the 28th week of gestation
- No social security coverage
- Refusal to be included
Sites / Locations
- Department of Gynecology Obstetrics and Reproductive Medicine, Hôpital Tenon, AP-HP, UPMC
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
A
B
Arm Description
sFlt-1 status known
sFlt-1 status unknown
Outcomes
Primary Outcome Measures
Reduction in the maternal and fetal morbimortality score
Secondary Outcome Measures
Child status
Length of hospital stay during pregnancy and post-partum periods
Predictive value for vascula-renal disease of urinary PlGF as compared with plasmatic sFlt-1.
Full Information
NCT ID
NCT00763672
First Posted
September 30, 2008
Last Updated
March 26, 2013
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT00763672
Brief Title
MorbiMortality Amelioration in Preeclamptic Primiparas Study. MoMA Pre Prim Study
Acronym
MOMA
Official Title
Impact of a Single Second-trimester Plasma sFlt-1 and/or Urinary PlGF Assay on Maternofetal Morbidity/Mortality
Study Type
Interventional
2. Study Status
Record Verification Date
March 2013
Overall Recruitment Status
Completed
Study Start Date
November 2008 (undefined)
Primary Completion Date
May 2011 (Actual)
Study Completion Date
June 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine whether close monitoring of patients with a high sFlt1 plasma level between 25 and 28 weeks of gestation (i.e. at high risk of subsequent preeclampsia) improves maternal and fetal outcomes. The investigator hypothesize that 1/ early screening for preeclampsia by plasmatic sFlt1 will reduce maternal and fetal mortality and morbidity and 2/ a simple urinary PlGF screening will be effective.
Detailed Description
We will measure plasmatic sFlt-1 level between 25 and 28 weeks of gestation and flow velocity of uterine arteries by Doppler (22 - 26 weeks of gestation) in primipara. Patients will be stratified according to the results of the uterine artery Doppler measurement, and then randomized in two groups A and B. In group A, sFlt-1 concentration will be communicated to the obstetrician (+ or -): the threshold of abnormally high plasmatic concentration of sFlt-1 is 957 ng/mL. In patients with a high plasmatic concentration of sFlt-1 (+), the pregnancy will be closely monitored including repeated clinical, biological, and ultrasound examinations. Patients with sFlt-1 plasmatic concentration below 957 ng/mL (-) will be routinely followed-up.In group B, the result of sFlt-1 measurement will not be communicated and the pregnancy will be routinely monitored.Abnormal Doppler recordings in either group will result in a close monitoring as per our usual local practice. Urinary PlGF (expressed as a ratio PlGF/creatininemia) will also be measured and the results will be analyzed at the end of the study. Beside sFlt-1, we will store the plasmatic samples to measure other biomarkers that could be relevant in the future (no DNA analysis will be done without a new patient consent).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pregnancy, Primiparity, Hypertension, Preeclampsia, Intrauterine Growth Retardation
Keywords
Preeclampsia, Hypertension, Intra uterine growth retardation, Antiangiogenic factor, Prevention
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1040 (Actual)
8. Arms, Groups, and Interventions
Arm Title
A
Arm Type
Other
Arm Description
sFlt-1 status known
Arm Title
B
Arm Type
Other
Arm Description
sFlt-1 status unknown
Intervention Type
Other
Intervention Name(s)
Transmission of sFlt-1 results to the investigator
Other Intervention Name(s)
Transmission of sFlt-1
Intervention Description
Transmission of sFlt-1 results by the laboratory to the investigator
Intervention Type
Other
Intervention Name(s)
No transmission of the sFlt-1 results to the investigator
Other Intervention Name(s)
No transmission of the sFlt-1
Intervention Description
The laboratory do not transmit the sFlt-1 results to the investigator before the end of the study.
Primary Outcome Measure Information:
Title
Reduction in the maternal and fetal morbimortality score
Time Frame
During the pregnancy and the 3 first month of the child
Secondary Outcome Measure Information:
Title
Child status
Time Frame
at 3 months post-delivery
Title
Length of hospital stay during pregnancy and post-partum periods
Time Frame
during pregnancy and post-partum periods
Title
Predictive value for vascula-renal disease of urinary PlGF as compared with plasmatic sFlt-1.
Time Frame
between 25 and 28 weeks of gestation
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Pregnant womenAge ≥ 18 years
Followed in our center before the 28th week of gestation
Under social security coverage
Signed informed consent
Exclusion Criteria:
Age < 18 years
Followed in our center after the 28th week of gestation
No social security coverage
Refusal to be included
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nadia BERKANE, MD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Gynecology Obstetrics and Reproductive Medicine, Hôpital Tenon, AP-HP, UPMC
City
Paris
ZIP/Postal Code
75020
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
15733721
Citation
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PubMed Identifier
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Citation
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PubMed Identifier
12618519
Citation
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Citation
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PubMed Identifier
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Citation
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Citation
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Citation
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Results Reference
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MorbiMortality Amelioration in Preeclamptic Primiparas Study. MoMA Pre Prim Study
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