Observational Study in UTERO - Placental 3D Doppler Examination: Interest for Pre-eclampsia Screening During Pregnancy
NCT ID: NCT00930397
Last Updated: 2020-12-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
146 participants
OBSERVATIONAL
2009-07-31
2011-11-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Low risk women
Women without any personal risk.
No interventions assigned to this group
High risk women
Women at high risk for pre-eclampsia with personal of pre-eclampsia and/or IUGR in a previous pregnancy, diabetes, auto-immune syndrome such as lupus, hypertension, renal insufficiency and anti-phospholipid.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Gestational age between 11 to 14 weeks for the first visit (first-trimester pregnancy).-Singleton pregnancy
* Consent to participate in the study
* Patients affiliated to social security
Group 1:
-Personal History of:
* Preeclampsia during a previous pregnancy: Blood pressure more than 140 mmHg systolic and/or 90 mmHg diastolic + proteinuria
* Diabetes
* IUGR during a previous pregnancy (birth weight \< 10th centile)
* Hypertension
* Renal insufficiency
* Autoimmune Disease : Antiphospholipid syndrome
Group 2:Absence of all the Group 1 affiliation criteria.
Exclusion Criteria
* Unability to understand the study
* Set back of patient consent.
18 Years
FEMALE
Yes
Sponsors
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GE Medical Systems ultrasound (only technical support)
UNKNOWN
Assistance Publique - Hôpitaux de Paris
OTHER
Responsible Party
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Principal Investigators
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Olivier MOREL, MD
Role: PRINCIPAL_INVESTIGATOR
Assistance Publique - Hôpitaux de Paris
Locations
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Hôpital LARIBOISIERE Service de gynécologie- obstétrique
Paris, , France
Countries
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Other Identifiers
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CRC 07049
Identifier Type: -
Identifier Source: org_study_id