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Clinical Trials/NCT04707105
NCT04707105
Recruiting
Not Applicable

A Prospective Observational Cohort Study in Chinese Patients With Primary Intracerebral Hemorrhage

Second Affiliated Hospital, School of Medicine, Zhejiang University1 site in 1 country856 target enrollmentDecember 29, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intracerebral Hemorrhage
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
Enrollment
856
Locations
1
Primary Endpoint
proportion of patients with a 3-month modified Rankin Scale (mRS) score≤ 3
Status
Recruiting
Last Updated
5 years ago

Overview

Brief Summary

The investigators design a prospective, observational cohort study to provide contemporary information on the prevalence, characteristics, risk stratification,cost-effective ,treatments and prognosis of Chinese hospitalised adult patients with intracerebral hemorrhage.

Detailed Description

Intracerebral hemorrhage (ICH) remains a devastating disease with high mortality, yet few therapeutic managements have been proved effective. Large quantities of work needs to be done to fully delineate the prevalence and prognosis of ICH. Hence, the investigators design a prospective, observational cohort study to provide contemporary information on the prevalence, characteristics, risk stratification,cost-effective, treatments and prognosis of Chinese hospitalised adult patients with ICH.

Registry
clinicaltrials.gov
Start Date
December 29, 2020
End Date
December 2026
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Hospitalized patients over 18 years old of primary intracerebral hemorrhage.

Exclusion Criteria

  • patients of secondary intracerebral hemorrhage,such as hemorrhagic transformation of ischemic stroke, aneurysmal, cavernomas, arterio- venous malformations, central venous thrombosis, trauma-related, or tumor.
  • isolated intraventricular hemorrhage or subarachnoid hemorrhage pregnant patients;
  • surgical evacuation of hematoma;
  • unavailability to get complete blood cell samples and presenting contraindications or refusal to MRI
  • patients cannot be followed up for any reasons.
  • patients death in 24 hours
  • pregnant patients

Outcomes

Primary Outcomes

proportion of patients with a 3-month modified Rankin Scale (mRS) score≤ 3

Time Frame: 2-3years

mRS 0-6, higher indicate worse outcome

Secondary Outcomes

  • Relative peripheral hematoma edema(rPHE)(2-3years)
  • National institute of health stroke scale(NIHSS score)(2-3years)
  • Absolute peripheral hematoma edema(PHE) growth(2-3years)

Study Sites (1)

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