N/A
18 Years
65 Years
18 Years
65 Years
Open (Enrolling)
Female
Premature Birth
Female
Premature Birth
Trial Information
Inclusion Criteria:
- Unique(only) or multiple pregnancy about is the term presenting an intra Utérine
pregnancy in the 1st quarter ·
- Signed lit(enlightened) consent ·
- Patient of more than 18 years old
Exclusion Criteria:
- Suspicion of pregnancy extra utérine, hémodynamique unstable, important métrorragies,
maternal diabetes, arterial high blood pressure
- impossibility to receive the consent lit(enlightened) by the patient · patient
old under age 18
Type of Study:
Interventional
Study Design:
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
Outcome Measure:
The elastography (elasticity imagery)
Outcome Time Frame:
18 months
Principal Investigator
Florence BRETELLE
Investigator Role:
Principal Investigator
Investigator Affiliation:
Assistance Publique Hopitaux De Marseille
Authority:
France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study ID:
2009-A00814-53
NCT ID:
NCT01032564
Start Date:
December 2009
Completion Date:
December 2011
Related Keywords:
- Premature Birth
- estimate the interest of the measure of cervix elasticity degree by elastography in prediction of premature birth within a population of pregnant women
- Premature Birth
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