De-Escalation of Dual Antiplatelet Therapy With Ticagrelor and Aspirin in Non-disabling Non-cardioembolic Ischemic Stroke or High Risk TIA Patients: A Randomized, Outcome Assessor Blind, Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2/Phase 3
SUMMARY

This is a randomized, controlled, outcome assessor blind, parallel group design pilot study on 100 patient with diagnosis of ischemic stroke admitted in Bou-Ali Sina Hospital, Sari,Iran.The aim of study is to compare the efficacy of 90 mg ticagrelor BID plus aspirin for 1 month and 60 mg ticagrelor BID plus aspirin for 6 months in reduce of non-disabling non-cardioembolic ischemic stroke or high risk TIA recurrence during first 12 months.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Healthy Volunteers: t
View:

• signing inform consent,

• recent ischemic stroke within 24 h,

• diagnosed by brain CT or MRI mild stroke with NIHSS =\<8 and no evidence of large infarct in brain imaging

• high risk TIA with ABCD \>4,

• no cardioembolic source such as low E/F, MS, AF ,...

• no specific etiology such as dissection, vasculitis, ...

• no carotid stenosis \> 50 % in side of involvement

Locations
Other Locations
Islamic Republic of Iran
Mazandaran province, Sari,Iran
RECRUITING
Sari
Contact Information
Primary
Athena Sharifi Razavi, MD
athena.sharifi@yahoo.com
+989113510136
Backup
Nasim Tabrizi, MD
nasimtabrizi@gmail.com
00989111263538
Time Frame
Start Date: 2024-04-01
Estimated Completion Date: 2026-08-01
Participants
Target number of participants: 100
Treatments
Experimental: intervention
Intervention group will be treat with ASA 325 mg stat and ticagrelor 180 mg stat, then ASA 80 mg daily and ticagrelor 90 mg BID for 30 days. Then ticagrelor 60 mg BID and ASA 80 mg daily until the end of month 6.
Active_comparator: comparator
Comparator group will be treat with ASA 325 mg stat and ticagrelor 180 mg stat, then ASA 80 mg daily and ticagrelor 90 mg BID for 30 days. Then ASA 80 mg daily until the end of month 6.
Related Therapeutic Areas
Sponsors
Leads: Mazandaran University of Medical Sciences

This content was sourced from clinicaltrials.gov