Evaluating outcomes of pregnancies with genital bleeding after 18 weeks
Maternal-fetal Outcomes of Genital Blood Loss Beyond 18 Weeks of Pregnancy
This study looks at how often serious problems happen in pregnancies with bleeding after 18 weeks to see if better ultrasound techniques can help doctors manage these cases.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 300 (estimated) |
| Ages | 18 Years to 45 Years |
| Sex | Female |
| Sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna Academic / other |
| Locations | 1 site (Bologna, Bologna) |
| Trial ID | NCT06802874 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the frequency of adverse maternal-fetal outcomes, such as premature birth and maternal-fetal hemorrhage, in pregnancies characterized by genital bleeding beyond 18 weeks. The study will analyze data collected from women attending the obstetric-gynaecological emergency department for this condition. Additionally, it seeks to evaluate the effectiveness of sonographic techniques in identifying the causes of genital bleeding over time, which may lead to improved management and individualized obstetrical care.
Who should consider this trial
Good fit: Ideal candidates for this study are pregnant women over 18 years of age who are experiencing genital bleeding beyond 18 weeks of gestation.
Not a fit: Patients who are not experiencing genital bleeding or are under 18 years of age will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of the risks associated with genital bleeding in late pregnancy, leading to better management strategies for affected patients.
How similar studies have performed: While this study addresses a specific aspect of maternal-fetal outcomes, similar observational studies have shown varying degrees of success in understanding complications related to pregnancy bleeding.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Bologna, Bologna
- IRCCS Azienda Ospedaliero-Universitaria di Bologna — Bologna, Bologna, Italy (Recruiting)
Study contacts
- Principal investigator: Elisa Morganti, MD — IRCCS Azienda Ospedaliero-Universitaria di Bologna
- Study coordinator: Elisa Montaguti, MD
- Email: elisa.montaguti@aosp.bo.it
- Phone: 0512144369
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.