Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT07270419

Aneurysmal Subarachnoid Hemorrhage Multi-Omics Research Program

Led by Xiaolin Chen, MD · Updated on 2025-12-08

2000

Participants Needed

1

Research Sites

213 weeks

Total Duration

On this page

Sponsors

X

Xiaolin Chen, MD

Lead Sponsor

P

Peking Union Medical College

Collaborating Sponsor

AI-Summary

What this Trial Is About

Aneurysmal subarachnoid hemorrhage (aSAH) is a life-threatening cerebrovascular emergency with high mortality and disability rates. Despite advances in neuroimaging and interventional techniques, outcomes remain poor for many patients due to complex post-rupture complications such as delayed cerebral ischemia (DCI), pneumonia, and other systemic injuries. These secondary events critically affect neurological recovery, yet their molecular mechanisms are not fully understood. This multicenter study aims to investigate the biological basis of post-rupture complications and prognosis in patients with aSAH through integrated multi-omics and clinical data analysis. Biospecimens including blood, cerebrospinal fluid, urine, and other relevant tissues will be collected for genomic, transcriptomic, proteomic, metabolomic, and imaging-omic profiling. By linking molecular data with clinical and imaging indicators, the study seeks to identify key pathways and biomarkers associated with secondary injury and outcome heterogeneity.

CONDITIONS

Official Title

Aneurysmal Subarachnoid Hemorrhage Multi-Omics Research Program

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients aged 6518 years
  • Confirmed diagnosis of aneurysmal subarachnoid hemorrhage (aSAH) by CTA or DSA
  • Aneurysm treated by microsurgical clipping or endovascular coiling during hospitalization
  • Time from onset to aneurysm treatment 64 72 hours
  • Availability of biospecimens including blood, cerebrospinal fluid, urine, or fecal samples collected during hospitalization
  • Signed informed consent from the patient or legal representative
Not Eligible

You will not qualify if you...

  • History of previous intracranial aneurysm surgery or embolization
  • Non-aneurysmal SAH, traumatic SAH, or perimesencephalic non-aneurysmal hemorrhage
  • Presence of malignancy, severe liver or kidney dysfunction, or other systemic diseases affecting survival or biomarker expression
  • Severe heart or lung failure or unstable medical condition preventing study participation
  • Pregnancy or breastfeeding
  • Refusal to participate or withdrawal of consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Beijing Tiantan Hospital

Beijing, Beijing Municipality, China, 100070

Actively Recruiting

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Research Team

R

Runting Li, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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