Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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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