National Research Center for Cardiac Surgery
Astana, 010000, Kazakhstan
Location status: Recruiting
NCT Number: NCT06874465
This study will analyze patients with aortic stenosis who have undergone transcatheter valve implantation and surgical aortic valve replacement. Afterwards, the results of these two procedures will be collected to the database and compared among the Kazakhstani population.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Astana, 010000, Kazakhstan
Location status: Recruiting
Primary Objectives
Study Design Registry, IV phase
Subject Follow-up Schedule Maximum follow-up is approximately 4 years.
Inclusion criteria
Patients have TAVI
Exclusion criteria
Patients have not TAVI
Primary Endpoints The database contains data on mortality, intraoperative complications, post-operative complications and adverse cardiovascular events. We will perform Quality of Life analysis before TAVI and one year later, using the Short-Form 36 (SF36) instrument on 70% of our patients.
Patient Safety The NRCCS is a leading center for interventional cardiology in Kazakhstan, and in Central Asia, performing a high volume of TAVI procedures annually
Procedure / Intervention Description
Secondary Endpoints
Statistical Method / Rationale Foundational work has been completed through our database development, but there is significant potential to expand our data collection to other Central Asian interventional cardiology centers. As technology evolves and options for trans-femoral TAVI approaches increase, the likelihood of using TAVI over SAVR will increase in Kazakhstan and Central Asia.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Compare self expendable and balloon expendable valves
Other names: Surgical aortic valve replacement
Time frame: 1 year
12 month all-cause of mortality
Time frame: 1 year
echocardiographic parameters: Aortic valve orifice area, aortic valve bioprosthetic gradient (peak, mean), aortic valve bioprosthetic velocity, ejection fracrion of left ventricle (LVEF%).
Time frame: within 30 days and 12 months
procedure associated stroke and 12 months
Time frame: within 30 days
procedure associated AB block which is need for permanent pacemaker implantation
Time frame: Baseline, 12 months
Quality of life on 36-item short-form (SF 36) will be carry before and 12 months after the procedure
Interested in participating?
Request InfoNational Research Center for Cardiac Surgery, Kazakhstan
Other
TAVI Registry at the National Research Center for Cardiac Surgery, Astana, Kazakhstan
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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