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Prediction Tool for Premature Labour and Neonatal Outcome (PRETURN)

G

Ghent University Hospital (UZ)

Status

Active, not recruiting

Conditions

Premature Birth

Study type

Observational

Funder types

Other

Identifiers

NCT03405116
B670201732321 (BC-00466)

Details and patient eligibility

About

A register and prediction model will be developed to predict the outcome of preterm labour and birth.

Enrollment

2,037 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Gestational age of 24 weeks 0 days and 33 weeks and 6 days, and their preterm born children

Exclusion criteria

  • Patients who choose not to participate in the research.
  • Intra-uterine prelabour fetal death.
  • Fetuses or neonates with a major congenital disorder. Major is defined as a disorder that has an impact on neonatal respiratory and cerebral outcome and/or long-term outcome.
  • Postpartum transfer/outborn.

Trial contacts and locations

1

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Central trial contact

Sara Somers; Isabelle Dehaene, MD

Data sourced from clinicaltrials.gov

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