BASAAspirin 81 mg vs 325 mg for Stroke Prevention in Head and Neck Vessels Injury
This study aims to compare the effectiveness of Aspirin 81 mg and 325 mg in preventing new stroke events (ischemic or hemorrhagic) in individuals with head and neck vessel injuries.
Aspirin 325Mg Tab, Aspirin 81Mg Tab
Prevention Study
Summary
Study start date: August 23, 2023
Actual date on which the first participant was enrolled.This clinical trial focuses on comparing the effectiveness of two different doses of Aspirin, 81 mg and 325 mg, in preventing strokes. The study involves patients who have experienced an injury to the blood vessels in their head and neck area. The main aim is to understand if the lower dose of Aspirin, 81 mg, is as effective as the higher dose, 325 mg, in stroke prevention. Additionally, the study also seeks to determine if the rate of bleeding complications is not higher in patients taking the lower dose. This research is important as it can help improve the care and treatment strategies for patients with such injuries. During the trial, participants are randomly assigned to take either Aspirin 81 mg or Aspirin 325 mg. The primary outcome being measured is the number of patients who experience a new stroke event, which could be either an ischemic stroke (caused by blood clots) or a hemorrhagic stroke (caused by bleeding in the brain). The study is designed to evaluate how well each dose of Aspirin prevents these events while also monitoring for any potential side effects or complications.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.98 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Prevention Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Loma Linda University Medical Center
Loma Linda, United StatesOpen Loma Linda University Medical Center in Google Maps