Ticagrelol Versus Aspirin in Ischemic Stroke
Primary Purpose
Acute Stroke, Ischemic Stroke
Status
Completed
Phase
Phase 3
Locations
Egypt
Study Type
Interventional
Intervention
Ticagrelor (Brilique) 90
Aspirin 75mg
Sponsored by
About this trial
This is an interventional treatment trial for Acute Stroke focused on measuring ticagrelol, aspirin
Eligibility Criteria
Inclusion Criteria:
- Male & female patients will be included
- Age between 18 - 75 years
- First ever presentation with acute ischemic stroke.Previous transient ischemic attacks (TIA's) are not excluding
- Ictus to drug time does not to exceed 9 hours.
Exclusion Criteria
- Patient eligible for recombinant tissue plasminogen activator (rTPA)
- patients with( national institute of health stroke scale (NIHSS) below 3 or above 25
- patients with active malignancy
- patients with major surgery in past 3 months
- patients with known allergy to study drugs
- patients with acute myocardial infarction in past 6 months
- patients known to suffer from multiple sclerosis or epilepsy
- pregnancy or lactation
- patients with history of head trauma with residual neurological deficits
- patients on regular ticagrelol in past week
- patients with international normalized ratio (INR) more than 1.3 or prothrombin time (PT) more than 18
- patients with venous thrombosis
- patients with platelet count less than 100000 or white blood cells (WBCs) less than 3000 or hematocrit value less than 0.25
- blood glucose less than 50 mg/DL or more than 400
Sites / Locations
- Neuropsychiatry department Kafrelsheikh university hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Ticagrelor ( Brilique) group
Aspirin Group
Arm Description
the group will receive 180 mg ticagrelor (2 tablets of 90 mg) as a single loading oral dose, and continue on 180 mg ticagrelor (1 tablet of 90 mg every 12 hours) for 3 months
The group will receive 300 mg Aspirin (4 tablets of 75 mg) as a single loading oral dose, and will then be commenced on 300 mg Aspirin daily for 2 weeks then 75 mg daily after that for 3 months
Outcomes
Primary Outcome Measures
hemorrhagic transformation of infarction within 48 hours of loading anti platelet in each group
hemorrhagic transformation detected by brain imaging CT and/or MRI brain will be done after 2 days of onset
amount of peripheral bleeding within 48 hours of loading anti platelet in each group
amount of peripheral bleeding measured in milliliter in each group
frequency of peripheral bleeding within 48 hours of loading anti platelet in each group
amount of peripheral bleeding measured as ( time per day )
Secondary Outcome Measures
difference between National institute of health stroke scale scores on admission and after one week in each group
National institute of health stroke scale ( NIHSS) difference between score on admission and after one week: we consider favorable outcome if there is decrease in NIHSS by 4 points or more this scale ranges from 0 to 42 . the higher the value the worse outcome with the following values: 1-4 Minor stroke 5-15 Moderate stroke 16-20 Moderate to severe stroke 21-42 Severe stroke
Modified Rankin scale in each group
Modified Rankin Scale (MRS): assessed at the end of 3 months , the higher the value the worse the outcome , MRS has following values :
0 = No symptoms at all
1= No significant disability despite symptoms
2= Slight disability
3= Moderate disability
4= Moderately severe disability
5= Severe disability; bedridden
6= Dead we consider favorable mRS if it was 2 or less
Mortality in each group
Timing and cause of death will be assessed
Full Information
NCT ID
NCT03884530
First Posted
March 8, 2019
Last Updated
August 30, 2021
Sponsor
Kafrelsheikh University
Collaborators
Ain Shams University
1. Study Identification
Unique Protocol Identification Number
NCT03884530
Brief Title
Ticagrelol Versus Aspirin in Ischemic Stroke
Official Title
Ticagrelol Versus Aspirin in Ischemic Stroke
Study Type
Interventional
2. Study Status
Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
May 1, 2019 (Actual)
Primary Completion Date
September 30, 2020 (Actual)
Study Completion Date
September 30, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kafrelsheikh University
Collaborators
Ain Shams University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
There is a debate whether ticagrelor is superior to aspirin in treating patients with ischemic stroke or not, most of the studies examine the effect of both drugs within 24 hours of acute stroke some find that there is no difference between ticagrelor and aspirin, others find that ticagrelor is superior to aspirin.
At this study the investigators aim at evaluating the role of loading ticagrelor received within 9 hours of acute ischemic stroke in improving neurological outcome of stroke. And evaluating the risk of hemorrhagic and non- hemorrhagic complications associated with the use of ticagrelor180 ml oral loading dose within 9 hours acute ischemic stroke
Detailed Description
ticagrelor is acyclo-pentyltriazolo-pyrimidine antiplatelet drug that inhibits the P2Y12which is a subtype of adenosine diphosphate (ADP)receptor.
It is a potent , direct-acting oral agent and it is reversibly binding P2Y12 receptors antagonist unlike the irreversible agents as clopidogrel, prasugrel, ticlopidine.
In 2011, the U.S. Food and Drug Administration (FDA) approved the blood-thinning drug (ticagrelor) to treat acute coronary syndromes, and in 2015, it approved it as long-term treatment in patient with history of heart attack.
In 2018, the American Heart Association ( AHA ) and American stroke Association (ASA) Guidelines for the Early Management of Patients with Acute Ischemic Stroke stated that, ticagrelor was not found to be superior to aspirin. However, because there were no significant safety differences, ticagrelor may be a reasonable alternative in stroke patients who have a contraindication to aspirin.
Aspirin overall reduces the risk of major vascular events by 13% Moreover, the risk of hemorrhagic events limits the use of aspirin in this setting, so the investigators aim at examining the hemorrhagic risks associated with use of loading Ticagrelor 180 ml within 9 hours of 1st ever acute ischemic stroke and compare the neurological outcomes in two groups of patients with 1st ever acute ischemic stroke receiving within 9 hours either Aspirin(300 mg (4 tablets of 75 mg) as a single loading oral dose, and will then be commenced on 300 mg Aspirin daily for 2 weeks then 75 mg daily after that for 3 months and the other received 180 mg ticagrelor (2 tablets of 90 mg) as a single loading oral dose, and continue on 180 mg ticagrelor (1 tablet of 90 mg every 12 hours) for 3 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Stroke, Ischemic Stroke
Keywords
ticagrelol, aspirin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Patients will be divided into 2 groups. The first group formed of 85 patients will receive 180 mg ticagrelor (2 tablets of 90 mg) as a single loading oral dose and continue on 180 mg ticagrelor (1 tablet of 90 mg every 12 hours). The second group formed of 84 patients will receive 300 mg Aspirin (4 tablets of 75 mg) as a single loading oral dose, and will then be commenced on 300 mg Aspirin daily for 2 weeks then 75 mg daily after that. If the patients showed complications of the loading dose of ticagrelor (central or peripheral bleeding the dose will be minimized to 90 mg (1 tablet of 90 mg).
Masking
None (Open Label)
Allocation
Randomized
Enrollment
169 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ticagrelor ( Brilique) group
Arm Type
Active Comparator
Arm Description
the group will receive 180 mg ticagrelor (2 tablets of 90 mg) as a single loading oral dose, and continue on 180 mg ticagrelor (1 tablet of 90 mg every 12 hours) for 3 months
Arm Title
Aspirin Group
Arm Type
Active Comparator
Arm Description
The group will receive 300 mg Aspirin (4 tablets of 75 mg) as a single loading oral dose, and will then be commenced on 300 mg Aspirin daily for 2 weeks then 75 mg daily after that for 3 months
Intervention Type
Drug
Intervention Name(s)
Ticagrelor (Brilique) 90
Intervention Description
Drug name Brilique 90 ml Drug form tablet
Intervention Type
Drug
Intervention Name(s)
Aspirin 75mg
Intervention Description
Drug name Aspirin 75 ml Drug form tablet
Primary Outcome Measure Information:
Title
hemorrhagic transformation of infarction within 48 hours of loading anti platelet in each group
Description
hemorrhagic transformation detected by brain imaging CT and/or MRI brain will be done after 2 days of onset
Time Frame
48 hours
Title
amount of peripheral bleeding within 48 hours of loading anti platelet in each group
Description
amount of peripheral bleeding measured in milliliter in each group
Time Frame
48 hours
Title
frequency of peripheral bleeding within 48 hours of loading anti platelet in each group
Description
amount of peripheral bleeding measured as ( time per day )
Time Frame
48 hours
Secondary Outcome Measure Information:
Title
difference between National institute of health stroke scale scores on admission and after one week in each group
Description
National institute of health stroke scale ( NIHSS) difference between score on admission and after one week: we consider favorable outcome if there is decrease in NIHSS by 4 points or more this scale ranges from 0 to 42 . the higher the value the worse outcome with the following values: 1-4 Minor stroke 5-15 Moderate stroke 16-20 Moderate to severe stroke 21-42 Severe stroke
Time Frame
one week or discharge
Title
Modified Rankin scale in each group
Description
Modified Rankin Scale (MRS): assessed at the end of 3 months , the higher the value the worse the outcome , MRS has following values :
0 = No symptoms at all
1= No significant disability despite symptoms
2= Slight disability
3= Moderate disability
4= Moderately severe disability
5= Severe disability; bedridden
6= Dead we consider favorable mRS if it was 2 or less
Time Frame
after one week and after 3 months
Title
Mortality in each group
Description
Timing and cause of death will be assessed
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male & female patients will be included
Age between 18 - 75 years
First ever presentation with acute ischemic stroke.Previous transient ischemic attacks (TIA's) are not excluding
Ictus to drug time does not to exceed 9 hours.
Exclusion Criteria
Patient eligible for recombinant tissue plasminogen activator (rTPA)
patients with( national institute of health stroke scale (NIHSS) below 3 or above 25
patients with active malignancy
patients with major surgery in past 3 months
patients with known allergy to study drugs
patients with acute myocardial infarction in past 6 months
patients known to suffer from multiple sclerosis or epilepsy
pregnancy or lactation
patients with history of head trauma with residual neurological deficits
patients on regular ticagrelol in past week
patients with international normalized ratio (INR) more than 1.3 or prothrombin time (PT) more than 18
patients with venous thrombosis
patients with platelet count less than 100000 or white blood cells (WBCs) less than 3000 or hematocrit value less than 0.25
blood glucose less than 50 mg/DL or more than 400
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hani Mohamed M Aref, MD
Organizational Affiliation
neuropsychiatry department Ain shams faculty of medicine
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Hala M Elkhawas, MD
Organizational Affiliation
neuropsychiatry department Ain shams faculty of medicine
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ahmed I Elbassiouny, MD
Organizational Affiliation
neuropsychiatry department Ain shams faculty of medicine
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Tamer M Roushdy, MD
Organizational Affiliation
neuropsychiatry department Ain shams faculty of medicine
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Hossam S Mohammed, MD
Organizational Affiliation
neuropsychiatry department Ain shams faculty of medicine
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Mohamed Zeinhom M Gomaa, M.Sc.
Organizational Affiliation
neuropsychiatry department Kafrelsheikh faculty of medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neuropsychiatry department Kafrelsheikh university hospital
City
Kafr Ash Shaykh
ZIP/Postal Code
33511
Country
Egypt
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
the individual participant data for all primary and secondary outcomes measures will be made available
IPD Sharing Time Frame
data will be available after 6 months of study completion
IPD Sharing Access Criteria
data access requests will be reviewed by an external independent review panel , requestors will be required to sign a data access agreement
Citations:
PubMed Identifier
27160892
Citation
Johnston SC, Amarenco P, Albers GW, Denison H, Easton JD, Evans SR, Held P, Jonasson J, Minematsu K, Molina CA, Wang Y, Wong KS; SOCRATES Steering Committee and Investigators. Ticagrelor versus Aspirin in Acute Stroke or Transient Ischemic Attack. N Engl J Med. 2016 Jul 7;375(1):35-43. doi: 10.1056/NEJMoa1603060. Epub 2016 May 10.
Results Reference
result
PubMed Identifier
34515113
Citation
Zeinhom MG, Aref HM, El-Khawas H, Roushdy TM, Shokri HM, Elbassiouny A. A pilot study of the ticagrelor role in ischemic stroke secondary prevention. Eur Neurol. 2022;85(1):50-55. doi: 10.1159/000518786. Epub 2021 Aug 30.
Results Reference
derived
Links:
URL
https://www.ncbi.nlm.nih.gov/pubmed/27160892
Description
https://www.ncbi.nlm.nih.gov/pubmed/27160892
Learn more about this trial
Ticagrelol Versus Aspirin in Ischemic Stroke
We'll reach out to this number within 24 hrs