Actively Recruiting
The Association Between a New Parameter Derived From DSA and Outcomes in Cerebral Ischemia
Led by Xi'an No.3 Hospital · Updated on 2023-09-01
30000
Participants Needed
1
Research Sites
521 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Ischemic cerebrovascular disease is a leading cause of death and disability worldwide. This study investigates a new parameter derived from Digital Subtraction Angiography (DSA) to evaluate cerebral blood flow and predict outcomes in patients with cerebral ischemia, specifically acute stroke with large vessel occlusion. Researchers aim to understand the relationship between this new DSA-based perfusion parameter and patient outcomes measured by the modified Rankin Scale. The study is observational and analyzes images from patients who have undergone DSA. Participants are classified based on their cerebral perfusion levels into good, middle, or poor perfusion groups using this new parameter. The study does not involve interventions but focuses on evaluating and comparing outcomes among these groups. Participants' DSA images and follow-up data on their clinical outcomes, collected between 3 months and 2 years after the procedure, will be analyzed. The main outcome measured is the difference in recovery and disability levels between patients with good and poor perfusion. Additional comparisons between good and middle perfusion groups will also be reviewed. The study is conducted by Xi'an No.3 Hospital and will continue until July 2038.
CONDITIONS
Brief Title
A New Parameter Derived From DSA to Evaluate Cerebral Perfusion
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of cerebral ischemia
- Patients who have undergone Digital Subtraction Angiography (DSA)
You will not qualify if you...
- Presence of cerebral hemorrhage
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single day
Participants undergo Digital Subtraction Angiography (DSA) to evaluate cerebral blood vessels and assess cerebral perfusion.
1 visit (in-person)
Duration - 3 months to 2 years
Participants are followed up to assess outcomes related to cerebral perfusion over time.
Periodic follow-up visits depending on clinical schedule
Trial Site Locations
Total: 1 location
1
Xi'an No.3 Hospital
Xi'an, Shaanxi, China, 710018
Actively Recruiting
Research Team
T
Tian Ye, doctor
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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