TIA Scores' Mortality Predictions and Recurrent TIA and Stroke Prediction

NCT06515392 | Recruiting

• 1 other identifier: TIA Scores and Mortality
• Study Type: observational
• Target: 300
• Locations: 1 country
• Sites: 1

Brief Summary

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

Stroke, Ischemic; Transient Ischemic Attack

Keywords

transient ischemic attack; ischemic stroke; TIA scores

Outcome Measures

Primary Outcomes (1)

• recurrent TIA or stroke

  recurrent TIA within 30 days of follow-up

  30 days

Study Arms (1)

TIA group

patients presenting with transient ischemic attack will be recorded and TIA scores and NIHSS score will be calculated, after 30 days follow-up, recurrent TIA and stroke rates will be determined

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

patients over the age of 18 presenting to emergency department with symptoms of stroke and diagnosed with TIA will be enrolled to study and will be followed up for 30 days for recurrent TIA or stroke

You may qualify if:

• 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

You may not qualify if:

• 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

Sponsors & Collaborators

• Saglik Bilimleri Universitesi: lead
• Ankara Etlik City Hospital: collaborator

Study Sites (1)

Etlik City Hospital

Ankara, Yenimahalle, 06170, Turkey (Türkiye)

RECRUITING

Related Publications (3)

• Perry JJ, Losier JH, Stiell IG, Sharma M, Abdulaziz K. National survey of emergency physicians for transient ischemic attack (TIA) risk stratification consensus and appropriate treatment for a given level of risk. CJEM. 2016 Jan;18(1):10-8. doi: 10.1017/cem.2015.57. Epub 2015 Jul 31.

  PMID: 26226855 BACKGROUND

• Cortel-LeBlanc MA, Sharma M, Cortel-LeBlanc A, Sivilotti MLA, Emond M, Stiell IG, Stotts G, Lee J, Worster A, Morris J, Cheung KW, Jin AY, Oczkowski WJ, Sahlas DJ, Murray HE, Mackey A, Verreault S, Camden MC, Yip S, Teal P, Gladstone DJ, Boulos MI, Chagnon N, Shouldice E, Atzema C, Slaoui T, Teitelbaum J, Abdulaziz KE, Wells GA, Taljaard M, Perry JJ. Predictors of neurologists confirming or overturning emergency physicians' diagnosis of TIA or stroke. CJEM. 2021 Nov;23(6):812-819. doi: 10.1007/s43678-021-00181-0. Epub 2021 Sep 1.

  PMID: 34468970 BACKGROUND

• Yang C, Jin A, Lin J, Wang Y, Xu J, Meng X. Validation of the Canadian TIA Score to Predict Subsequent Stroke Risk in Chinese TIA Patients. Cerebrovasc Dis. 2022;51(6):735-743. doi: 10.1159/000524264. Epub 2022 May 5.

  PMID: 35512630 BACKGROUND

MeSH Terms

Conditions

Ischemic Stroke; Ischemic Attack, Transient

Condition Hierarchy (Ancestors)

Stroke; Cerebrovascular Disorders; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Vascular Diseases; Cardiovascular Diseases; Brain Ischemia

Study Officials

• gulsen akcay, ass. prof.

  ass. prof. of organization

  STUDY DIRECTOR

Central Study Contacts

gulsen akcay, ass. prof.

CONTACT

+905052874949; gulakcay@yahoo.com.tr

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Target Duration: 30 Days
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 17, 2024
• First Posted: July 23, 2024
• Study Start: June 1, 2024
• Primary Completion: June 1, 2025
• Study Completion: June 1, 2025
• Last Updated: July 23, 2024

Record last verified: 2024-07

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)