Observational study on intracerebral hemorrhage in hospitalized adults

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to gather contemporary data on the prevalence, characteristics, risk factors, and prognosis of hospitalized adult patients in China suffering from primary intracerebral hemorrhage (ICH). It is a prospective, observational cohort study that will analyze various aspects of ICH, including treatment approaches and cost-effectiveness. The goal is to enhance understanding of this serious condition, which has high mortality rates and limited effective treatments. By focusing on a specific patient population, the study seeks to provide valuable insights into ICH management.

Why it matters

Who can join: the full rules

Inclusion Criteria:

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

Exclusion Criteria:

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

Where it's running

• 2nd Affiliated Hospital, School of Medicine at Zhejiang University
  Hangzhou, Zhejiang, China Recruiting

Study contacts

• Principal investigator: Feng Gao, MD,PhD — Second Affiliated Hospital, Zhejiang University, School of Medicine
• Study coordinator: Feng Gao, MD,PhD
• Email: 2202012@zju.edu.cn
• Phone: 13588451471

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.