Estimation of the Placental Volume by 3D Ultrasound at 12, 16 and 22 Weeks : Relation With Growth Factors and D-Dimers
NCT ID: NCT00767182
Last Updated: 2016-03-23
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
40 participants
OBSERVATIONAL
2008-08-31
2009-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Pregnant patients with VPP antecedent
Pregnancy women consulting for an scan during their 12th week of amenorrhea at the University Hospital of Saint Etienne will be studied in this clinical trial. They have an history of VPP (Vascular Placental Pathology). They will have to give a blood sample.
blood sample
biological markers evaluated : D-Dimer, sEPCR
Interventions
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blood sample
biological markers evaluated : D-Dimer, sEPCR
Eligibility Criteria
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Inclusion Criteria
* coming for a 12 weeks ultrasound
Exclusion Criteria
* past history of in utero fetal death due to congenital malformations, rhesus incompatibility or an infection
* previous history of IUGR which etiology was a chromosomal, genic or infectious anomaly
18 Years
50 Years
FEMALE
No
Sponsors
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Groupe de Recherche sur la Thrombose
OTHER
Centre Hospitalier Universitaire de Saint Etienne
OTHER
Responsible Party
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Principal Investigators
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Céline CHAULEUR, MD
Role: PRINCIPAL_INVESTIGATOR
CHU de Saint-Etienne
Locations
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Service de Gynécologie Obstétrique - CHU Saint-Etienne
Saint-Etienne, , France
Countries
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Other Identifiers
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2008-A00233-52
Identifier Type: OTHER
Identifier Source: secondary_id
DGS2008-0193
Identifier Type: OTHER
Identifier Source: secondary_id
0808025
Identifier Type: -
Identifier Source: org_study_id
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