Actively Recruiting

Age: 18Years - 80Years
All Genders
Healthy Volunteers
ID06906432

Multimodal Omics and Imaging Study on Brain-Heart Injury Mechanisms in Patients With Intracranial Hemorrhage

Led by Beijing Tiantan Hospital · Updated on 2025-04-02

1000

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

Sponsors

B

Beijing Tiantan Hospital

Lead Sponsor

B

Beijing Youyi Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating the mechanisms behind brain and heart injuries in patients who suffer from intracranial hemorrhage, a serious condition with high death rates and poor recovery outcomes. This condition causes direct brain damage and secondary problems like delayed cerebral ischemia, brain swelling, and fluid buildup. It can also lead to cardiac issues classified as cerebrocardiac syndrome, which includes heart attacks, abnormal heart rhythms, and heart dysfunction, all linked to worse patient outcomes. The exact causes of these brain and heart injuries remain unclear, and this study aims to explore these processes to improve diagnosis and treatment. Participants with intracranial hemorrhage will receive usual care alongside detailed multidisciplinary assessments involving blood and cerebrospinal fluid tests, electrocardiograms, ultrasounds, and imaging scans. The study is observational and uses a combined approach of advanced omics and imaging methods to examine both local brain and systemic injuries. This approach seeks to enhance precise diagnosis, risk evaluation, and clinical decision-making. During the study, researchers will monitor short- and long-term cardiac events, delayed cerebral ischemia, and brain-heart syndrome up to three months after discharge. Functional outcomes will be assessed using the modified Rankin Scale at discharge and three months later. Participants will be evaluated within five days of admission and followed up at three months to collect comprehensive data on their brain and heart health, helping to understand the injury mechanisms and patient recovery over time.

CONDITIONS

Brief Title

Mechanisms of Brain-Heart Injury of Post-Intracranial Hemorrhage

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years or older at the time of enrollment
  • Acute intracranial hemorrhage confirmed by neuroimaging (CT, MRI, CTA, MRA, or DSA) within 48 hours of symptom onset
  • Ability to provide informed consent or have a legally authorized representative willing to consent on their behalf
Not Eligible

You will not qualify if you...

  • Patients who refuse to participate or cannot provide informed consent
  • History of significant cardiovascular disease including myocardial infarction, heart failure, or arrhythmias unless stable and well-controlled
  • Cardiac bypass surgery, stent placement, or other cardiovascular interventions within the past 6 months
  • Active brain tumors, ischemic stroke within 3 months, or previous brain injury that could affect study results
  • Active malignant disease, severe inflammatory or infectious disease, or recent surgery within the past 3 months
  • Any condition making participation unsafe or impractical as judged by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 5 days

Participants undergo multi-disciplinary assessments including blood tests, cerebrospinal fluid tests, electrocardiograms, ultrasound, and imaging to evaluate brain-heart injury mechanisms.

Assessments conducted during hospital stay up to discharge

Long-term Monitoring

Duration - 3 months post-discharge

Participants are monitored for long-term cardiac events, delayed cerebral ischemia, and brain-heart syndrome, as well as functional outcomes over 3 months post-discharge.

Follow-up visits or assessments up to 3 months after discharge

Trial Site Locations

Total: 1 location

1

Beijing Tiantan Hospital Affiliated to Capital Medical University

Beijing, Beijing Municipality, China, 100070

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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