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

ConditionBlood Loss
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna

About this trial

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 criteria

Qualifiers

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

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed