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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
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

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

First Posted
September 30, 2008
Last Updated
March 26, 2013
Sponsor
Assistance Publique - Hôpitaux de Paris
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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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Citation
Nagamatsu T, Fujii T, Kusumi M, Zou L, Yamashita T, Osuga Y, Momoeda M, Kozuma S, Taketani Y. Cytotrophoblasts up-regulate soluble fms-like tyrosine kinase-1 expression under reduced oxygen: an implication for the placental vascular development and the pathophysiology of preeclampsia. Endocrinology. 2004 Nov;145(11):4838-45. doi: 10.1210/en.2004-0533. Epub 2004 Jul 29.
Results Reference
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PubMed Identifier
15622693
Citation
Familoni OB, Adefuye PO, Olunuga TO. Pattern and factors affecting the outcome of pregnancy in hypertensive patients. J Natl Med Assoc. 2004 Dec;96(12):1626-31.
Results Reference
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PubMed Identifier
12618519
Citation
Maynard SE, Min JY, Merchan J, Lim KH, Li J, Mondal S, Libermann TA, Morgan JP, Sellke FW, Stillman IE, Epstein FH, Sukhatme VP, Karumanchi SA. Excess placental soluble fms-like tyrosine kinase 1 (sFlt1) may contribute to endothelial dysfunction, hypertension, and proteinuria in preeclampsia. J Clin Invest. 2003 Mar;111(5):649-58. doi: 10.1172/JCI17189.
Results Reference
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PubMed Identifier
12538598
Citation
Sugimoto H, Hamano Y, Charytan D, Cosgrove D, Kieran M, Sudhakar A, Kalluri R. Neutralization of circulating vascular endothelial growth factor (VEGF) by anti-VEGF antibodies and soluble VEGF receptor 1 (sFlt-1) induces proteinuria. J Biol Chem. 2003 Apr 11;278(15):12605-8. doi: 10.1074/jbc.C300012200. Epub 2003 Jan 21.
Results Reference
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PubMed Identifier
12618513
Citation
Luttun A, Carmeliet P. Soluble VEGF receptor Flt1: the elusive preeclampsia factor discovered? J Clin Invest. 2003 Mar;111(5):600-2. doi: 10.1172/JCI18015. No abstract available.
Results Reference
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PubMed Identifier
12727995
Citation
Koga K, Osuga Y, Yoshino O, Hirota Y, Ruimeng X, Hirata T, Takeda S, Yano T, Tsutsumi O, Taketani Y. Elevated serum soluble vascular endothelial growth factor receptor 1 (sVEGFR-1) levels in women with preeclampsia. J Clin Endocrinol Metab. 2003 May;88(5):2348-51. doi: 10.1210/jc.2002-021942.
Results Reference
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PubMed Identifier
18175241
Citation
Romero R, Nien JK, Espinoza J, Todem D, Fu W, Chung H, Kusanovic JP, Gotsch F, Erez O, Mazaki-Tovi S, Gomez R, Edwin S, Chaiworapongsa T, Levine RJ, Karumanchi SA. A longitudinal study of angiogenic (placental growth factor) and anti-angiogenic (soluble endoglin and soluble vascular endothelial growth factor receptor-1) factors in normal pregnancy and patients destined to develop preeclampsia and deliver a small for gestational age neonate. J Matern Fetal Neonatal Med. 2008 Jan;21(1):9-23. doi: 10.1080/14767050701830480.
Results Reference
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Citation
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PubMed Identifier
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Citation
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
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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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