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A Cohort Study of Patients With Intracranial Hemorrhage

C

Capital Medical University

Status

Enrolling

Conditions

Intracerebral Hemorrhage

Treatments

Other: Routine clinical treatment

Study type

Observational

Funder types

Other

Identifiers

NCT05760950
Cohort Study for ICH

Details and patient eligibility

About

As one of the most serious forms of acute stroke, the early mortality rate of intracerebral hemorrhage(ICH) can be as high as 30-40%. The incidence of intracerebral hemorrhage increases with the increase of age. Under the circumstance of the aggravation of aging in China, intracerebral hemorrhage brings a certain burden to families and society.

The results of several studies in recent years have failed to provide new therapeutic approaches for the treatment of cerebral hemorrhage. Therefore, novel therapeutic approaches is urgently needed for ICH. Primary and secondary prevention, acute inpatient care, and poststroke rehabilitation are all critical. The objective of this cohort study is to explore factors that might influence the long-term prognosis of patients with ICH and to further identify new potential targets for intervention.

Full description

The observational cohort study will be used to find the possible treatment methods and predictors of functional outcome. The medical records of patients will be collected, including age, sex, comorbid conditions, toxic habits, use of medications (antiplatelets, anticoagulants, and antihypertensives), systolic and diastolic blood pressure, Glasgow Coma Scale (GCS) score, and National Institutes of Health Stroke Scale (NIHSS) score on admission. Image data will also be collected. Follow-up information will be obtained from the medical records or telephone interviews.

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Primary intracerebral hemorrhage
  • Over 18 year-old

Exclusion criteria

  • Secondary intracerebral hemorrhage, such as aneurysmal, hemorrhagic transformation of ischemic stroke, cavernomas, arterio-venous malformations, central venous thrombosis, trauma-related, or tumor.
  • Pregnant patients.
  • Any condition which, in the judgment of the investigator, might increase the risk to the patient.

Trial contacts and locations

1

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Central trial contact

Xunming Ji; Mengke Zhang

Data sourced from clinicaltrials.gov

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