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Recruiting Observational

Maternal-fetal Outcomes of Genital Blood Loss Beyond 18 Weeks of Pregnancy

NCT06802874 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2023-11-15
Last updated
2025-01-31

Condition(s) studied

Blood Loss

Study summary

The primary objective is to assess in terms of frequency the adverse outcomes (premature birth, maternal-fetal haemorrhage, maternal fetal-neonatal death) of pregnancies of women attending the obstetric-gynaecological emergency department for genital bleeding beyond the 18th week of pregnancy.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
45 Years
Healthy volunteers
No
Inclusion Criteria: * Pregnancy beyond 18 weeks gestational age complicated by genital bleeding; * Age of the patient ≥18 years; * Delivery at the O.U. of Obstetrics and Prenatal Age Medicine Exclusion Criteria: None

Primary outcome measure(s)

  • Rate of hospitalization for genital blood loss — After the 18th week of pregnancy
  • Percentage of preterm births — After delivery, up to 24 weeks
  • Percentage of spontaneous deliveries, operative vaginal, cesarean sections (elective, urgent, emergent) — After delivery, up to 24 weeks
  • Frequency of antihemorrhagic therapy and maternal transfusions — Intra-partum and post-partum, up to 24 weeks
  • Frequency of live births, average APGAR, average pH of umbilical artery or vein, average neonatal weight — After delivery, up to 24 weeks
  • Average length of hospitalization in hours — During Hospitalization, up to 24 weeks

Trial sites (1)

FacilityCityRegionStatus
IRCCS Azienda Ospedaliero-Universitaria di Bologna Bologna Bologna Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06802874 on ClinicalTrials.gov ↗ ← All trials in Italy