Aortic StenosisTAVI(Transcatheter Aortic Valve Implantation)Computed TomographyInflammatory Response During Cardiac SurgeryInflammation
Investigational drug(s) / intervention(s)
laboratory biomarker analysisComputed tomography of aortic root and aorta
laboratory biomarker analysis: Results of common laboratory tests obtained during routine care in the pre-procedural period (simple blood morphology, creatinine, GFR, NTproBNP). Inflammatory indices - NLR, MLR, PLR
Computed tomography of aortic root and aorta: Results of CT analysis performed as a routine diagnostic examination in the pre-procedural period will be recorded.
Study summary
The aim of the project is to evaluate demographic, clinical, and laboratory variations in patients with aortic stenosis treated with TAVI in different countries. Moreover, the study will evaluate interpopulation differences in aortic root anatomy based on computed tomography analysis.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Severe aortic stenosis qualified for TAVI
Exclusion Criteria:
* Active infection (chronic inflammatory disease or neoplasm is not an exclusion criterion, however, will be considered in the laboratory analysis)
Primary outcome measure(s)
Aortic annulus diameter — Baseline Aortic annulus diameter in milimeters based on CT image
Aortic annulus area — Baseline Aortic annulus area in squared milimeters based on CT image
Aortic annulus perimeter — Baseline Aortic annulus perimeter in milimeters based on CT image
Ilio-femoral artery diameter — Baseline Ilio-femoral artery diameter in milimeter based on CT image
Neutrophils measured using whole blood count — Baseline This measurement is used to compute ratio of cell types using whole blood count
Monocytes measured in whole blood count — Baseline Number of monocytes identified in blood sample using automatic whole blood count. It is used to compute cell type ratio.
Lymphocytes measured using whole blood count — Baseline This measurement is used to compute ratio of cell types using whole blood count
Trial sites (5)
Facility
City
Region
Status
San Bortolo's Hospital, Division of Cardiac Surgery and Division of Cardiology, Vicenza, Italy
Vicenza
Italy
Poznan University of Medical Sciences
Poznan
Poland
Institute for Cardiovascular Diseases of Vojvodina, Serbia University of Novi Sad
Novi Sad
Serbia
King Chulalongkorn Memorial Hospital, Bangkok, Thailand
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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