Actively Recruiting

Age: 18Years +
All Genders
NCT06515392

TIA Scores' Mortality Predictions and Recurrent TIA and Stroke Prediction

Led by Saglik Bilimleri Universitesi · Updated on 2024-07-23

300

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

S

Saglik Bilimleri Universitesi

Lead Sponsor

A

Ankara Etlik City Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Our study adopts a prospective design. Our research aims to determine the significance of ABCD2, ABCD3-I, Canadian TIA Score, and NIHSS Score in predicting the likelihood of ischemic stroke within 30 days in patients presenting to the emergency department with transient ischemic attack (TIA)

CONDITIONS

Official Title

TIA Scores' Mortality Predictions and Recurrent TIA and Stroke Prediction

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients presenting to the emergency department and diagnosed with TIA
  • Patients diagnosed with ischemic stroke who did not receive thrombolytic therapy based on NIHSS score
  • Patients aged 18 and above
  • Patients who consented by signing the informed consent form
Not Eligible

You will not qualify if you...

  • Patients diagnosed with hemorrhagic stroke
  • Patients unwilling to participate in the study
  • Patients with a history of trauma
  • Patients unable to receive thrombolytic therapy for any reason (trauma, malignancy, etc.)
  • Patients under the age of 18
  • Patients transferred from another hospital
  • Patients who experienced cardiac arrest
  • Patients who died for any reason other than ischemic stroke within 30 days
  • Patients wishing to withdraw from the study at any time during the study period

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Etlik City Hospital

Ankara, Yenimahalle, Turkey (Türkiye), 06170

Actively Recruiting

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Research Team

G

gulsen akcay, ass. prof.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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