Actively Recruiting
Manual- VS Auto-Strain
Led by Bruno Mora · Updated on 2026-03-27
70
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Myocardial strain analysis provides additional and valuable information about left ventricular function, particularly in the perioperative setting with its dynamic changes in ventricular load conditions. This allows for earlier risk assessment and, if necessary, the initiation of faster and more targeted therapy. Unfortunately, conventional strain analysis using conventional methods currently takes approximately 5 minutes. However, this amount of time is often not available in a dynamically changing intraoperative setting during cardiac surgery. Therefore, the benefits of strain analysis have not yet been routinely utilized during the intraoperative course. However, new software solutions exist that can perform strain analysis fully automatically and reduce the examination time to a few seconds. However, it remains unclear whether these fully automated analyses also function reliably intraoperatively using transesophageal echocardiography (TEE). The aim of this study is to assess the reliability of these new methods.
CONDITIONS
Official Title
Manual- VS Auto-Strain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult (≥18 years) cardiac surgery patients
- Sinus rhythm
- No severe valvular regurgitation
- Use of General Electric echocardiography systems (Vivid S60, S70, E95) and EchoPAC software along with TOMTEC software
You will not qualify if you...
- Inadequate image quality
- Any severe heart valve regurgitation
- Use of mechanical circulatory support systems (e.g., LVAD, Impella, ECMO)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
General Hospital of Vienna - Medical University of Vienna
Vienna, Austria, 1090
Actively Recruiting
Research Team
B
Bruno Mora, Dr, MD, PhD
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
0
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