Clinical Trials in Italy / NCT06802874
Recruiting
Observational
Maternal-fetal Outcomes of Genital Blood Loss Beyond 18 Weeks of Pregnancy
NCT06802874 · tracked via the Priya Life Science Italy tracker
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| IRCCS Azienda Ospedaliero-Universitaria di Bologna | Bologna | Bologna | Recruiting |
More IRCCS Azienda Ospedaliero-Universitaria di Bologna trials in Italy
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