CClinicalTrials.gg
RecruitingNCT06880107GENANXVAUpdated Jan 16, 2026

Genetic Variants of Annexin A2 and Cryptogenic Stroke

An interventional study of blood withdrawal in Annexin A2, Stroke and Genetic Variants of Host, sponsored by Centre Hospitalier Universitaire, Amiens. Recruiting at 1 site in France. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-16.

Sponsored by Centre Hospitalier Universitaire, Amiens · Not applicable, Interventional, and Screening

From the registry’s dates

  • Started Apr 2025; still recruiting 1 year 6 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
240
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

Stroke is the third most common cause of death in developed countries. Various mechanisms of ischemic stroke exist. However, in young population, in a third of cases, the cause of a stroke cannot be determined despite an extensive evaluation. Many studies have highlighted the link between stroke and fibrinolysis. Genetic variants of tPA and PAI-1 genes have been suggested to be the risk factors for stroke.

ANXA2 plays a pivotal role in plasmin generation and fibrinolysis. Several studies showed the role of ANXA2 and S100A10 subunits in regulation of fibrinolysis in vivo. Recently, the efficacy of recombinant ANXA2 for fibrinolytic therapy in a rat embolic stroke has been demonstrated. Some single nucleotide polymorphisms in ANXA2 gene could be associated with increased risk of stroke in sickle cell disease.

Therefore, these data invite us to test hypothesis that genetic variants of ANXA2 gene could be associated with ischemic stroke.

02

Conditions studied

  • Annexin A2
  • Stroke
  • Genetic Variants of Host
  • Fibrinolysis

Browse trials for

Keywords

  • annexin A2
  • stroke
  • genetic variants
  • fibrinolysis
03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's planned enrollment of 240 is above the median of 50 across 5,369 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Centre Hospitalier Universitaire, Amiens is the lead sponsor of 576 studies on the registry; 178 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

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

Exclusion Criteria:

  • Transient ischemic attack
  • Pregnancy
05

Study design

Phase
Not applicable
Primary purpose
Screening
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
240 participants (estimated)

Study arms

  • Experimental
    cryptogenic stroke

    cryptogenic stroke

    Biological: blood withdrawal

  • Experimental
    ischemic stroke

    ischemic stroke

    Biological: blood withdrawal

  • Active comparator
    control subjects

    control subjects

    Biological: blood withdrawal

Interventions

  • Biologicalblood withdrawal

    blood withdrawal

06

What researchers measure

Primary outcomes

  1. genetic variants of ANXA2

    Time frame: day 1

  2. genetic variants of S100A10

    Time frame: day 1

Secondary outcomes

  1. blood ANXA2 concentration

    Time frame: day 1

  2. blood S100A10 concentration

    Time frame: day 1

  3. concentration of Autoantibodies directed against ANXA2

    Time frame: day 1

  4. concentration of S100A10 directed against ANXA2

    Time frame: day 1

07

Study locations

1 of 1 sites recruiting
  • CHRU Amiens
    Amiens, 80054, France
    • Valéry Salle, MD · Contact · salle.valery@chu-amiens.fr · 33+3 22 66 82 30
    • Olivier GODEFROY, Pr · Sub investigator
    • Sandrine CANAPLE, MD · Sub investigator
    • Chantal LAMY, MD · Sub investigator
    • Audrey ARNOUX COURSELLE, MD · Sub investigator
    • Estelle CADET, rPH · Sub investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06880107
Lead sponsor
Centre Hospitalier Universitaire, Amiens
Responsible party
Sponsor
First posted
Mar 17, 2025
Start date
Apr 8, 2025
Primary completion
Apr 2027 (estimated)
Completion
Apr 2027 (estimated)
Last update
Jan 16, 2026

Study contacts

Valéry SALLE, MD
Contact
salle.valery@chu-amiens.fr
33+3 22 66 82 30

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion