Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact
Recruiting Observational

Transpacific TAVR Registry

NCT03826264 · tracked via the Priya Life Science South Korea tracker
Sponsor
Duk-Woo Park, MD
Phase
Observational
Started
2019-06-15
Last updated
2026-01-02

Condition(s) studied

Heart Valve DiseasesAortic Valve Insufficiency

Investigational drug(s) / intervention(s)

TAVR

TAVR: transcatheter aortic valve replacement (TAVR)

Study summary

This registry evaluates the long-term outcome of Transcatheter aortic valve replacement (TAVR) in real-world clinical practice.

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * All patients undergoing TAVR * Informed consent

Primary outcome measure(s)

  • Event rate of all cause death — 1 year

Trial sites (7)

FacilityCityRegionStatus
Stanford University Stanford California Recruiting
Northwestern Memorial Hospital Chicago Illinois Recruiting
Second Affiliated Hospital of Zhejiang University Hangzhou China Recruiting
Bucheon Sejong Hospital Bucheon-si South Korea Active Not Recruiting
Chungnam National University Hospital Daejeon South Korea Recruiting
Asan Medical Center Seoul South Korea Recruiting
Seoul National University Hospital Seoul South Korea Completed
Official registry record

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.

View NCT03826264 on ClinicalTrials.gov ↗ ← All trials in South Korea