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Clinical Trials in China / NCT06670456
Recruiting Observational

Prospective Cohort of Patients With Intracerebral Hemorrhage

NCT06670456 · tracked via the Priya Life Science China tracker
Sponsor
De-zhi Kang
Phase
Observational
Started
2023-11-06
Last updated
2024-11-01

Condition(s) studied

Stroke, AcuteIntracerebral Hemorrhage

Study summary

The investigators designed a multicentral, observational, prospective cohort study to provide cortical data for risk stratification and biomarkers on early outcomes, complications, long-term neurological function, and cognitive status of spontaneous intracerebral hemorrhage patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Diagnosed with spontaneous intracerebral hemorrhage (ICH) through skull radiologic scans (CT or MRI); * Underwent no surgical intervention; Exclusion Criteria: * Secondary intracerebral hemorrhage (with leading cause, e.g., Moyamoya disease, arteriovenous malformation, intracranial aneurysm, tumor, brain trauma) * Pre-stroke life expectancy \< 1 year for severe comorbidities (e.g., Progressive malignant tumor, severe chronic heart failure \[NYHA: III-IV\], severe chronic obstructive pulmonary disease \[III-IV\], chronic kidney disease requiring hemodialysis) * Severe dependency or incorporation to interview (e.g., pre-stroke mRS\>3, severe dementia, intractable mental disease) * Unsuitable for inclusion in the study in the opinion of the investigator

Primary outcome measure(s)

Trial sites (6)

FacilityCityRegionStatus
First Affiliated Hospital of Fujian Medical University Fuzhou Fujian Recruiting
Anxi County Hospital Quanzhou Fujian Recruiting
Jinjiang Municipal Hospital Quanzhou Fujian Recruiting
The Second Affiliated lospital of Xiamen Medical College Xiamen Fujian Recruiting
Zhangzhou Municipal Hospital Zhangzhou Fujian Recruiting
Liaocheng People's Hospital Liaocheng Shandong Recruiting

Other trials for the same condition

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 NCT06670456 on ClinicalTrials.gov ↗ ← All trials in China