Status:
COMPLETED
Identification of Spontaneous Delivery Markers
Lead Sponsor:
Assistance Publique - Hôpitaux de Paris
Collaborating Sponsors:
URC-CIC Paris Descartes Necker Cochin
Conditions:
Preterm Labor (24 GA - 32 GA)
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
The investigators project aims to identify, in pregnant women, discriminating molecules to allow an early detection of women who will spontaneously deliver prematurely, suitable in routine clinical pr...
Detailed Description
Prematurity is a major Public Health concern in developed countries, since it is the first cause of perinatal morbi-mortality and of cerebral palsy in early childhood. Premature birth rate has risen b...
Eligibility Criteria
Inclusion
- \- Singleton pregnancy, monitored in Port Royal or secondarily transferred, between 24 and 32 GA. Hospitalization for preterm labor (cervix \< 25 mm at transvaginal cervical ultrasound) or -Singleton pregnancy, monitered in Port Royal between 15-16 weeks of gestation, without complication.
- or - Singleton pregnancy, monitered in Port Royal between 35-36 weeks of gestation, without complication.
- or - Healthy woman, no pregnancy.
Exclusion
- Minor
- Not affiliated to health insurance
- Persons under guardianship or judicial protection
- Infection with HIV, Hepatitis B Virus (HBV) or Hepatitis C Virus (HCV)
- Diabetes or chronic inflammatory disease
- Carrier of B streptococcus
- Cervical strapping
- Fetus with chromosomal abnormalities
- Infections
- Premature rupture of membrane
Key Trial Info
Start Date :
December 14 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 16 2018
Estimated Enrollment :
238 Patients enrolled
Trial Details
Trial ID
NCT02225717
Start Date
December 14 2014
End Date
April 16 2018
Last Update
December 11 2025
Active Locations (1)
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1
Maternité Port Royal-Cochin
Paris, France, 75014