Predicting the progressive adverse events of intracerebral hemorrhage through interpretable AI-driven spatiotemporal evolution of the environment

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2600122454

Enrollment

Unknown

Registered

2026-04-14

Start date

2026-05-01

Completion date

Unknown

Last updated

2026-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral hemorrhage

Interventions

Observation group:None

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients confirmed by imaging as having spontaneous intracranial hemorrhage within 24 hours of the onset of symptoms

Exclusion criteria

Exclusion criteria: 1. Patients with intracranial hemorrhage caused by trauma or suspected trauma before the onset of symptoms; 2. Patients with secondary intracranial hemorrhage, such as those with tumors, aneurysms, vascular malformations, and hemorrhagic transformation after cerebral infarction;

Design outcomes

Primary

Measure	Time frame
Receiver operating characteristic curve (ROC);Area Under the ROC Curve(AUC);	—

Secondary

Measure	Time frame
The volume of the hematoma within 72 hours after the patient's bleeding;Death rate;Modified Rankin Scale(mRS);Activities of Daily Living(ADL);	—

Countries

China

Contacts

Public ContactLin Jie

The First Affiliated Hospital of Wenzhou Medical University

5337518@qq.com+86 577 5557 8777

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026