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NCT04971564Recruiting

Thrombo-inflammation Biomarkers Trial in Acute Cerebral Hypoxia

Thrombo-inflammation Biomarkers Trial in Acute Cerebral Hypoxia. A Case-control Trial Nested in a Cohort

Source: ClinicalTrials.gov · Last updated 22 Jan 2026

Brief summary (registry, in English)

The goal of this trial is to study, in three well-defined clinical situations responsible for cerebral hypoxia, the concentrations of biomarkers of thrombo-inflammation compared to a population of patients without cerebral hypoxia, and to study in patients with cerebral hypoxia the association between these concentrations and the clinical evolution.

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
12 Jul 2021
Start date
19 Mar 2024
Primary completion date
22 Jun 2026
Lead sponsor
Fondation Ophtalmologique Adolphe de Rothschild
Diseases
Stroke
NCT number
NCT04971564

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 19 Mar 2024 to the primary completion date, 22 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients diagnosed with an acute non-vascular neurological pathology (migraine, epilepsy, etc.).

Other

  • Pre-existing functional and/or cognitive disability
  • Patient under legal protection.
  • Pregnant or breastfeeding woman.
  • Patient with secondary haemorrhagic transformation.
    • Secondary exclusion criteria :
  • Patients with an ischaemic lesion visible on imaging, unrelated to large vessel occlusion and therefore ineligible for mechanical thrombectomy.
  • TIA patients presenting an abnormality on follow-up imaging 24-48 hours after the initial imaging.
    • Excluded patients will be replaced.

Who the study is looking for

  • \- For cases, admitted within the first 36 hours of an acute neurological symptom related to :
  • An ischaemic cerebrovascular accident (iCVA) eligible for a mechanical thrombectomy procedure,
  • A subarachnoid haemorrhage (SAH, all aetiologies) : patient presenting with at least a modified Fisher scale 3 or 4,
  • An intra-parenchymal haematoma (IPH) with greatest axis ≥ 20mm or with NIHSS on admission \>4.
    • OR
  • For control patients, admitted within 7 days of the onset of acute neurological symptomatology related to a clinical diagnosis of transient ischaemic attack (TIA) - based on thorough questioning of the patient on admission - and prior to imaging, with an ABCD2≥ 2 score.
  • Express consent to participate in the study.
  • Member or beneficiary of a social security.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hopital Fondation Adolphe de Rothschild
Coordinator of this site? Confirm its status
ParisFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.