Actively Recruiting
A Point-of-care Electrochemical-based Device for Rapid Detection of Fibrinogen on Type A Aortic Dissection Surgery
Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2025-05-15
150
Participants Needed
1
Research Sites
73 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study compares the results of the existing fibrinogen concentration monitoring technology to the Electrochemical-based device, a point-of-care and rapid method,using a small amount of extra blood obtained in Type A Aortic Dissection Surgery.
CONDITIONS
Official Title
A Point-of-care Electrochemical-based Device for Rapid Detection of Fibrinogen on Type A Aortic Dissection Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Subject is 18 years or older
- Subject underwent surgery for acute type A aortic dissection at the hospital
- Subject requires routine thromboelastography (TEG) measurement
- Subject uses human fibrinogen concentrate during surgery
You will not qualify if you...
- Use of extracorporeal membrane oxygenation (ECMO) after surgery
- Inability to provide written informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The Second Affiliated Hospital of Zhejiang University anesthesiology department
Hangzhou, Zhejiang, China, 310009
Actively Recruiting
Research Team
F
Fengjiang ZHANG
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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