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NCT06670456Recruiting

Prospective Cohort of Patients With Intracerebral Hemorrhage

Multicentral Observational Prospective Cohort of Patients With Spontaneous Intracerebral Hemorrhage

Source: ClinicalTrials.gov · Last updated 1 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
3000 (estimated)
First submitted
31 Oct 2024
Start date
6 Nov 2023
Primary completion date
31 Dec 2027
Lead sponsor
De-zhi Kang
Diseases
Stroke
NCT number
NCT06670456

What you commit to

  • Study type: Observational
  • Planned participants: 3000
  • From 6 Nov 2023 to the primary completion date, 31 Dec 2027
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 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)

Other

  • Unsuitable for inclusion in the study in the opinion of the investigator

Who the study is looking for

  • Diagnosed with spontaneous intracerebral hemorrhage (ICH) through skull radiologic scans (CT or MRI);
  • Underwent no surgical intervention;

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
First Affiliated Hospital of Fujian Medical University
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FuzhouChinaRecruiting
Liaocheng People's Hospital
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LiaochengChinaRecruiting
Jinjiang Municipal Hospital
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QuanzhouChinaRecruiting
Anxi County Hospital
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QuanzhouChinaRecruiting
The Second Affiliated lospital of Xiamen Medical College
Coordinator of this site? Confirm its status
XiamenChinaRecruiting
Zhangzhou Municipal Hospital
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ZhangzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.