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NCT Number: NCT06874465

Transcatheter Aortic Valve Implantation Registry at the National Research Center for Cardiac Surgery, Nur-Sultan, Kazakhstan

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

National Research Center for Cardiac Surgery

Astana, 010000, Kazakhstan

Location status: Recruiting

Location contact

Abdurashid Mussayev, PhD

CONTACT

[email protected]

+77029997667

Aidyn Kuanyshbek, MD

SUB_INVESTIGATOR

Marat Aripov, PhD

SUB_INVESTIGATOR

Nursultan Tanaliyev, MD

SUB_INVESTIGATOR

Serik Alimbayev, PhD

PRINCIPAL_INVESTIGATOR

Timur Lesbekov, PhD

PRINCIPAL_INVESTIGATOR

About this study

Primary Objectives

  • Prevalence of aortic stenosis in Kazakhstan regions
  • 12 months survival of patients after TAVI
  • Intra- and postoperative complications
  • Conduction disorders after TAVI
  • Left ventricle function after TAVI in patients with low ejection fraction
  • Comparison of aortic route dimensions by 3D-TEE and MSCT
  • Comparison of TAVR with SAVR

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

  • We believe our database is unique because it is the first systematically-collected, prospectively designed database in Central Asia for patients receiving TAVI.
  • As known there is no data has been published regarding TAVI in Central Asia.

Secondary Endpoints

  • Surgeons at NRCCS tend to use biological valves over mechanical valves because it was recognized that the requirements for long term success of mechanical valves (e.g. warfarin maintenance and compliance) were unlikely to be achieved in our patient population, many of whom live in rural areas without access to advanced cardiology care.
  • Some of these patients are now returning to our center for valve in valve implantation and are being included in our registry. • 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.

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Transcatheter aortic valve implantation

Device

Compare self expendable and balloon expendable valves

Other names: Surgical aortic valve replacement

Primary outcomes

  1. Number of death

    Time frame: 1 year

    12 month all-cause of mortality

  2. Evaluate of echocardiographic results

    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%).

  3. Incidence of stroke

    Time frame: within 30 days and 12 months

    procedure associated stroke and 12 months

  4. Permanent pacemaker implantation

    Time frame: within 30 days

    procedure associated AB block which is need for permanent pacemaker implantation

Secondary outcomes

  1. Life quality

    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

Study contacts

Contact information is provided by the study sponsor or research team.

Abdurashid Mussayev, PhD

CONTACT

[email protected]

+77029997667

Sadyk Khamitov

CONTACT

[email protected]

+77055756439

Sponsors and collaborators

Lead sponsor

National Research Center for Cardiac Surgery, Kazakhstan

Other

Collaborators

  • Medtronic Cardiovascular

Registry information

Official study title

TAVI Registry at the National Research Center for Cardiac Surgery, Astana, Kazakhstan

Important dates

Study start
2020
Primary completion
2021
Study completion
2026
First posted
Mar 13, 2025
Registry last updated
Mar 13, 2025

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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