Clinical trial Recruiting at 1 site Observational Ages 18 to 80

Identifying biomarkers and imaging markers for intracerebral hemorrhage

Official title: Biomarkers and Imaging Markers Screening for Intracerebral Hemorrhage Patients

Run by Southwest Hospital, China · NCT06462274 · Data updated 2026-11-12

This study is trying to find new blood and imaging tests that can help doctors better understand and treat patients who have had a severe type of stroke called intracerebral hemorrhage.

More Intracerebral Hemorrhage trials

Quick facts

Study typeObservational
Ages18 Years to 80 Years
SexAll
Enrollment200 (estimated)
SponsorSouthwest Hospital, China
Academic / other
Locations1 site (Chongqing, Chongqing Municipality)
StatusRecruiting
StartedJanuary 1, 2014
Main results expectedJune 1, 2026
Study endsDecember 1, 2026
Registry record updatedJune 17, 2024
Trial IDNCT06462274 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18-80 years with a spontaneous intracerebral hemorrhage confirmed by CT scan and a hematoma size greater than 5 ml.

Probably not a fit

Patients with ICH due to aneurysms, arteriovenous malformations, tumors, or trauma, as well as those with severe organ dysfunction, will not benefit from this study.

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

What this trial studies

This observational study focuses on intracerebral hemorrhage (ICH), a severe type of stroke that leads to high mortality and disability. Researchers aim to discover potential biomarkers by analyzing blood, cerebrospinal fluid, urine, saliva, and tissue samples from ICH patients, alongside conducting multimodal imaging scans such as CT, MRI, MRS, and PET. The goal is to enhance understanding of the pathophysiological mechanisms of ICH and develop new tools for diagnosis, monitoring, and prognosis. By correlating molecular and imaging markers, the study seeks to improve therapeutic decisions and risk stratification for affected patients.

Why it matters

Potential benefit: If successful, this study could lead to improved diagnostic and therapeutic strategies for patients suffering from intracerebral hemorrhage.

How similar studies have gone: While the approach of identifying biomarkers and imaging markers is promising, it remains largely novel and untested in the specific context of intracerebral hemorrhage.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Individuals aged 18-80 years
2. Hematoma size is more than 5 ml
3. Evidence of a spontaneous ICH on CT scan
4. Patient within 72 hours of ictus
5. Glasgow Coma Scale (GCS) Score of 5-15.
6. The history of hypertension

Exclusion Criteria:

1. Individuals with age \< 18 years or \> 80 years
2. Clear evidence that the hemorrhage is due to an aneurysm, arteriovenous malformation or other cerebrovascular diseases.
3. ICH secondary to tumor or trauma..
4. If the haematological effects of any previous anticoagulants are not completely reversed.
5. Patients with heart insufficiency, lungs insufficiency, renal insufficiency, hepatic insufficiency, autoimmune diseases and other organ diseases with severe dysfunction.

Where it's running

  • Department of Neurosurgery , Southwest Hospital, Third Military Medical University,
    Chongqing, Chongqing Municipality, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.