Annexin A2 (ANXA2) gene variants and ischemic stroke risk

Is this trial a fit for you?

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

What this trial studies

Researchers will enroll adults with a completed ischemic stroke and collect a blood sample for DNA analysis. The DNA will be genotyped to identify single nucleotide variants in the ANXA2 gene and related loci. Genotype frequencies will be compared with expected population patterns or correlated with clinical stroke features to see if specific variants are overrepresented. The work is conducted at CHRU Amiens and excludes transient ischemic attack and pregnant participants.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Completed ischemic stroke defined as a rapidly developing focal neurologic deficit with no apparent cause other than a vascular origin that persisted beyond 24 hours in surviving patients
* Age from 18 years old

Exclusion Criteria:

* Transient ischemic attack
* Pregnancy

Where it's running

• CHRU Amiens
  Amiens, France Recruiting

Study contacts

• Study coordinator: Valéry SALLE, MD
• Email: salle.valery@chu-amiens.fr
• Phone: 33+3 22 66 82 30

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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.