The Assessment Of Myocardial Viability Based On CTA/MRI Hybrid Models
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- STATUS
- Recruiting
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- participants needed
- 100
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- sponsor
- Cardio Med Medical Center
Summary
The aim of HYBRIDHEART study is to develop new imagistic prototype for a complex
Description
The HYBRIDHEART study is a prospective, observational study that will be conducted in the Laboratory of Advanced Research in Cardiac Multimodal Imaging of Cardio Med Medical Center Trgu Mure, Romania.
The project will include 100 subjects with documented ST Segment elevation myocardial
The imagistic acquisitions obtained from all the techniques used, will be processed using a
supercomputer set up with computational simulations applications for the myocardial kinetics.
All the MRI images will be analyzed using Medis Q-mass software in order to quantify the
The study will be conducted over a period of 2 years, in which the subjects will be examined
at the moment of inclusion and during the follow-up visits. Will be performed the follow up
of the subjects at 1, 3 and 6 months and 1 year after the inclusion period. At 1 month follow
up the subjects will be examined, will be performed
Study objectives:
Primary: to develop new imagistic markers for a complex
Secondary: to evaluate the association of the percent of viable myocardium with the level of
inflammatory markers. To correlate the
Study
Baseline (day0) Obtain a written consent from the participants on study consent form. Verify
inclusion/exclusion criteria Assess the demographical data of the participants, medical
history, possible known
Visit 1 (month 1) Physical examination record
Visit 2 (month 3) Telephone visit with target questions, all the answers recorded in study forms.
Visit 3 (month 6) End point
Visit 4 (12 months) End point
Study procedures:
Clinical examinations
MRI for the
Data collection:
A dedicated database will be created, including all the demographical data and data regarding
the
Details
Condition |
Coronary Artery |
---|---|
Age | 18years - 90years |
Treatment |
Speckle Tracking |
Clinical Study Identifier | NCT04397198 |
Sponsor | Cardio Med Medical Center |
Last Modified on | 19 February 2024 |
How to participate?
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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