Registry of patients undergoing transcatheter aortic valve implantation in Kazakhstan
Official title: TAVI Registry at the National Research Center for Cardiac Surgery, Astana, Kazakhstan
Run by National Research Center for Cardiac Surgery, Kazakhstan · NCT06874465 · Data updated 2026-11-12
This study looks at patients in Kazakhstan who have had aortic valve surgery to see how well they do and how their quality of life changes over time.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | National Research Center for Cardiac Surgery, Kazakhstan Academic / other |
| Locations | 1 site (Astana) |
| Status | Recruiting |
| Started | January 10, 2020 |
| Main results expected | January 10, 2021 |
| Study ends | January 10, 2026 |
| Registry record updated | March 13, 2025 |
| Trial ID | NCT06874465 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients diagnosed with severe symptomatic aortic stenosis who are undergoing TAVI.
✕Probably not a fit
Patients with active endocarditis or a recent history of cerebrovascular events may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This registry analyzes patients with aortic stenosis who have undergone transcatheter aortic valve implantation (TAVI) and surgical aortic valve replacement (SAVR) in Kazakhstan. The study aims to collect and compare outcomes, including survival rates, complications, and quality of life, over a follow-up period of up to four years. It will also assess the prevalence of aortic stenosis in different regions of Kazakhstan and evaluate the effectiveness of TAVI compared to SAVR. This is the first systematically collected database for TAVI in Central Asia.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the outcomes of TAVI in the Kazakhstani population, potentially improving patient care and treatment strategies.
How similar studies have gone: While this approach is novel for Central Asia, similar registries in other regions have shown success in improving patient outcomes and understanding of TAVI.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients has given written informed Concent for study participation prior to procedure * Patients with Aortic Valve stenosis * Patients has severe degenerative or congenital aortic stenosis. * Patients has symptomatic aortic stenosis as demonstrated by NYHA II or greater Exclusion Criteria: * Patients has active endocarditis * Patients has history of cerebral vascular accident or transient ischemic attack within the past 3 months
Where it's running
-
National Research Center for Cardiac Surgery
Astana, Kazakhstan Recruiting
Study contacts
- Study coordinator: Abdurashid Mussayev, PhD
- Email: abdurashid.mussayev@gmail.com
- Phone: +77029997667
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Transcatheter Aortic Valve Replacement Registry for Outcomes and Quality Monitoring
This registry collects information from hospitals about patients undergoing TAVR to see how care and outcomes compare to guidelines and nationwide data.
-
Vericiguat to slow calcific aortic valve narrowing
This trial tests whether vericiguat can slow the progression of mild-to-moderate calcific aortic valve stenosis compared with placebo.
-
CHATEAU Registry: Real-world outcomes after TAVR
This registry collects real-world data from adults who had TAVR between 2021 and 2025 to see how they do over time and how valve performance holds up.
-
Impact of TAVR on kidney function in people with aortic valve disease
This registry tests how trans-catheter aortic valve implantation affects kidney function and the risk of kidney injury in adults with aortic stenosis.
-
Hydra THV Transfemoral Valve Implantation in Severe Aortic Stenosis
This registry tests how safely and effectively the Hydra THV works when implanted through the femoral artery in adults with severe symptomatic aortic stenosis.
-
How the type of sedation affects recovery after TAVR
This study will test whether three common sedation approaches (propofol, dexmedetomidine, or midazolam with fentanyl) change how people recover on the first day after transfemoral TAVR.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.