Clinical Trials in Italy / NCT06782802
Recruiting
Observational
Clinical Significance and Prognostic Value of Prenatal Diagnosis of Obliteration of the Cavum Septum Pellucidum
NCT06782802 · tracked via the Priya Life Science Italy tracker
Condition(s) studied
Fetal Neurodevelopmental DisorderCavum Septum Pellucidum
Study summary
The aim of this observational study is to evaluate the incidence of the occurrence of additional abnormalities in fetuses diagnosed with cavum septum pellucidum (CSP) obliteration performed at second-trimester ultrasound, as well as to analyze the postnatal neurological outcome.
Eligibility
Inclusion Criteria:
* Pregnant participants with a diagnosis of cavum septum pellucidum obliteration made at second-trimester morphologic ultrasound between 19+0 and 21+6 weeks
* Age \> or = 18 years at the time of outpatient access
* Acquisition of informed consent form, from the patient and minor
* Patients followed at our center
Exclusion Criteria:
* None
Primary outcome measure(s)
- Assessment of the incidence of brain abnormalities — During second-trimester ultrasound
Evaluation of the incidence of associated brain abnormalities, diagnosed by neurosonography and MRI, both at the time of diagnosis and found at subsequent planned follow-ups until the end of pregnancy in fetuses with a finding of obliteration of the cavum septum pellucidum
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 NCT06782802 on ClinicalTrials.gov ↗ ← All trials in Italy