Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID07270419

Aneurysmal Subarachnoid Hemorrhage Multi-Omics Research Program (aSAH-Omics): A Multicenter Clinical and Mechanistic Study

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

2000

Participants Needed

1

Research Sites

52 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 serious brain emergency caused by a ruptured aneurysm, leading to high death and disability rates. Despite improvements in imaging and treatment techniques, many patients face poor outcomes due to complications like delayed cerebral ischemia, pneumonia, and other systemic injuries. These secondary problems greatly affect recovery, but the molecular causes are not yet fully clear. This multicenter study aims to explore the biological reasons behind these complications and recovery differences by combining multi-omics data with clinical information in patients with aSAH. The study collects various biospecimens such as blood, cerebrospinal fluid, urine, and other tissues to analyze genomic, transcriptomic, proteomic, metabolomic, and imaging-related data. Patients who have had their aneurysm treated by microsurgical clipping or endovascular coiling within 72 hours of the hemorrhage are included. This research links molecular data with clinical and imaging results to identify key pathways and biomarkers that relate to secondary brain injury and patient outcomes. Participants will be assessed over time with functional outcomes measured by the Modified Rankin Scale at 3, 6, and 12 months after the hemorrhage. Secondary outcomes include rates of rebleeding, delayed cerebral ischemia, anemia, pneumonia, and deep vein thrombosis within the first 30 days or up to 3 months. Biospecimen collection during hospitalization supports detailed analysis. This observational study involves long-term follow-up to better understand the biological basis of aSAH progression and recovery variability.

CONDITIONS

Brief 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 618 years
  • Confirmed aneurysmal subarachnoid hemorrhage diagnosis by CTA or DSA
  • Aneurysm treated by microsurgical clipping or endovascular coiling during hospitalization
  • Treatment performed within 72 hours from hemorrhage onset
  • Availability of biospecimens including blood, cerebrospinal fluid, urine, or fecal samples
  • Signed informed consent by patient or legal representative
Not Eligible

You will not qualify if you...

  • History of previous intracranial aneurysm surgery or embolization
  • Non-aneurysmal subarachnoid hemorrhage, traumatic SAH, or perimesencephalic non-aneurysmal hemorrhage
  • Malignancy, severe liver or kidney dysfunction, or other systemic diseases affecting survival or biomarkers
  • Severe heart or lung failure or unstable medical condition preventing participation
  • Pregnancy or lactation
  • Refusal or withdrawal of consent

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)

Monitoring

Duration - Up to 3 months after hemorrhage onset

Participants who have experienced aneurysmal subarachnoid hemorrhage are observed with collection of clinical data and biospecimens to study post-rupture complications and recovery.

Visits and sample collections occur during hospitalization and follow-up up to 3 months

Long-term Monitoring

Duration - Up to 12 months after hemorrhage onset

Participants are followed to assess functional outcomes and long-term recovery after the hemorrhage.

Follow-up visits at 3, 6, and 12 months

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

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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