Actively Recruiting
Predicting Cerebrovascular Adverse Events Post Cardiac Surgery
Led by IRCCS Policlinico S. Donato · Updated on 2025-03-28
104
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
Sponsors
I
IRCCS Policlinico S. Donato
Lead Sponsor
U
University of Milan
Collaborating Sponsor
AI-Summary
What this Trial Is About
The aims of this study are: i) to assess cerebral autoregulation and autonomic control within the different phases of cardiac surgery with cardiopulmonary bypass; ii) to compare cerebral autoregulation measures derived via cerebral blood flow velocity estimated by transcranial Doppler device with simpler measurements derived from near infrared spectroscopy; iii) to develop a predictive model of postoperative cerebrovascular outcome (overt or silent stroke) based on the extracted indices.
CONDITIONS
Official Title
Predicting Cerebrovascular Adverse Events Post Cardiac Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age older than 18 years
- Spontaneous sinus rhythm
- Not pregnant
- Signed informed consent
You will not qualify if you...
- Age lower than 18 years
- Absence of sinus rhythm
- Autonomic disorders
- Concomitant carotid intervention
- Reintervention
- Contraindication to MRI
- Pregnancy
- Inability to provide informed consent
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
IRCCS Policlinico San Donato
San Donato Milanese, Milan, Italy, 20097
Actively Recruiting
Research Team
V
Vlasta Bari, Ph.D.
CONTACT
G
Giacomo Bortolussi, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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