About this trial
The goal of this observational study is to train a machine learning system based on data from patients affected by spontaneous Intracranial Hemorrage. The main question it aims to answer is whether there is a correlation between actual clinical pratice, reached outcomes and favorable or unfavorable predictive factors, and anamnesis.
Participants will be treated as per standard clinical practice.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients who enter the NICU for acute spontaneous intracranial hemorrhage
Adult patients (≥ 18 years)
Sex: female, male, intersex
Disqualifiers
All patients affected by non-spontaneous ICH
Patients with sICH determined by brain tumor or brain metastases
All patients affected by chronic ICH
Pregnant and puerperal women
Trial population
All patients affected by spontaneous Intracranial Hemorrhage.
Trial design
Cohort
Cross-sectional
Treatments tested in this trial
Treatment of spontaneous intracranial hemorrhage
Other interventionData collection of therapeutic approach, including radiological, medical, surgical therapies.
Treatment groups
Trial outcomes
Primary outcomes
Mortality
Patients who die within 12 months after being treated for spontaneous intracranial hemorrhage
Sponsors and contacts
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