Status:

COMPLETED

New Biomarkers Associated With the Risk of Premature Delivery.

Lead Sponsor:

University Hospital, Bordeaux

Conditions:

Premature Delivery

Eligibility:

FEMALE

18+ years

Phase:

NA

Brief Summary

Despite the progress made in the organization of care and neonatal care, prematurity remains the main cause of morbidity and perinatal mortality. This study aims to estimate the prognostic value of n...

Detailed Description

Despite the progress made in the organization of care and neonatal care, prematurity remains the main cause of morbidity and perinatal mortality. With 7.2% of premature deliveries in France, threat of...

Eligibility Criteria

Inclusion

  • Pregnant women over 18 years of age
  • Term from 22 to 33 and 6 amenorrhea weeks
  • Single or twin pregnancy
  • Emergency consultant, in participating centers, for a threat of premature labor defined by:
  • Uterine contractions greater than or equal to 3 in 30 minutes Clinical modification of the cervix Ultrasound collar less than 25 mm
  • Free, informed and written consent, dated and signed by the patient and the investigator before any investigation required by the research.
  • Patient affiliated to a Social Security scheme.

Exclusion

  • Premature rupture of membranes
  • Placenta previa
  • Vaginal haemorrhage at the time of sampling
  • Uterine malformation
  • Strapping, open bite
  • History of strapping and or open bite
  • Conization
  • Fetal malformation
  • Associated vasorenal pathology
  • Sexual intercourse less than 24h
  • Gynecological examination less than 48h
  • Vaginal treatment in progress
  • Polyhydramnios
  • Transfused-transfused syndrome
  • Twin Anemia Polycythemia syndrome
  • Fetoscopy during pregnancy

Key Trial Info

Start Date :

June 7 2011

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 28 2013

Estimated Enrollment :

182 Patients enrolled

Trial Details

Trial ID

NCT04067908

Start Date

June 7 2011

End Date

December 28 2013

Last Update

August 28 2019

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