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BIO-PREDISC-TIA SWISS Cohort Study

BIOmarkers and PREDISC Diagnostic Evaluation for Patients With Suspected Transient Ischemic Attacks: the BIOPREDISC- TIA SWISS Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03994003
Acronym
PREDISC
Enrollment
64
Registered
2019-06-21
Start date
2017-08-04
Completion date
2021-12-31
Last updated
2024-04-18

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

Conditions

Cerebrovascular Disease, Ischemic Stroke

Brief summary

This research project aims at contributing to improve TIA diagnosis and management by using PREDISC scores and specific biomarkers thought to have elevated levels in TIA patients. A swift and accurate TIA diagnosis allows starting treatment of the patient adequately and shortly after the event. The shorter the time between the event and treatment onset, the better the outcome. This approach will be an important step forward in TIA diagnosis and management, similarly to acute coronary syndrome as discussed above.

Interventions

None listed

Sponsors

Ente Ospedaliero Cantonale, Bellinzona
CollaboratorOTHER
Dr. med. Carlo Cereda
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Patients with suspected TIA (defined as the acute onset of focal neurological symptoms lasting \<24 h and presumed to be caused by brain ischemia at the time of referral) within 48 h of symptoms onset. * At least 18 years old. * Having given their Informed Consent.

Exclusion criteria

* · Patients with ocular TIA (Amaurosis fugax). * Patients that still have neurological deficits at the moment of inclusion. * Contraindication to perform MRI. * For women: pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Levels of specific biomarkers (Platelet Basic Protein (PBP), ceruloplasmin, microRNAs, exosomal particles) in patients with suspected TIA.1 yearDiagnostic performance according to PREDISC scale

Countries

Switzerland

Outcome results

None listed

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