Skip to content

Biomarkers for the Diagnosis of Transient Ischemic Attack

Biomarkers for the Diagnosis of Transient Ischemic Attack

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02799511
Acronym
MAESTRO
Enrollment
25
Registered
2016-06-15
Start date
2015-03-31
Completion date
2019-09-30
Last updated
2021-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebrovascular Disorders, Ischemic Attack, Transient

Keywords

biological markers

Brief summary

A transient ischemic attack (TIA) should be considered an emergency prevention opportunity in order to avoid recurrence as cerebral infarction (CI) serious (fatal or disabling). Indeed, about 20% of patients who have IC had in previous days or weeks, a TIA, which can be defined as a brief episode of cerebral dysfunction (or eye) do not result in permanent brain damage and thus no sequelae. Moreover, about 20% of ischemic events observed in practice are AIT. Despite the progress achieved in the treatment in the acute phase of an IC, prevention remains the most effective way to fight against this disease. This prevention can be put in place before the occurrence of a first IC, or after a first IC, especially when minor as a TIA. However, the diagnosis of TIA remains particularly difficult and it is necessary now to identify new tools for the diagnosis of transient ischemic attack. Our study focused on the identification of one or more molecules (called biological markers or biomarkers) present in the bloodstream of patients, which will serve to facilitate the differential diagnosis of patients with TIA.

Interventions

BIOLOGICALprotein expression

Differential protein expression between the period of acute cerebral ischemia and the control period

Sponsors

University Hospital, Caen
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* TIA lasting 18h * NIHSS \< 0 * MRI diffusion hypersignal less than 5 ml * follow up during 3 month * written informed consent prior to any study procedures

Exclusion criteria

* Pregnant or breastfeeding women * major comorbidity (cancer, chronic infection) * recent trauma (less than 30 days) (cranial or extracranial) * Surgical or endovascular recent surgery(within 30 days). * Any old brain injury * Any acute pathology likely to induce inflammation, hemostasis disorders ... * Contraindications to MRI: Patients with a pacemaker, an implanted material activated by an electrical, magnetic or mechanical carriers hemostatic clips intracerebral aneurysms or carotid arteries, bearing orthopedic implants, claustrophobic ... * Patient under guardianship

Design outcomes

Primary

MeasureTime frameDescription
change in proteomic analysis from MPs or from plasma.baseline and 72h after TAI and 90 days after TAIIdentify one or more markers of transient ischemic attack by a proteomic analysis from MPs or from plasma.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026