Viewing Study NCT06503965



Ignite Creation Date: 2024-10-26 @ 3:35 PM
Last Modification Date: 2024-10-26 @ 3:35 PM
Study NCT ID: NCT06503965
Status: RECRUITING
Last Update Posted: None
First Post: 2024-07-10

Brief Title: Tunisian Registry of Trans Catheter Aortic Valve Implantation
Sponsor: None
Organization: None

Study Overview

Official Title: Design and Rationale of the National Multicenter Tunisian Registry of Trans Catheter Aortic Valve Implantation Registry
Status: RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: TAVI-TN
Brief Summary: Transcatheter aortic valve implantation TAVI has emerged as a transformative therapy for patients with severe aortic stenosis particularly those designated high-risk or inoperable for traditional surgical valve replacement Despite its increasing adoption worldwide there re-mains a paucity of data regarding TAVI outcomes in Tunisian patients In response to this gap in knowledge the investigators propose the establishment of the Tunisian TAVI Registry a multicenter initiative aimed at comprehensively documenting the clinical characteristics procedural de-tails and short- and long-term outcomes of TAVI procedures across Tunisia The TAVITN registry will enroll consecutive patients undergoing TAVI procedures at participating centers across Tunisia between 2013 and 2024 with a retrospective arm and a prospective arm The TAVI-TN Registry represents a significant step towards enhancing our understanding of TAVI outcomes in the Tunisian population By systematically capturing real-world data this initiative aims to inform clinical decision-making improve patient care and contribute to the advancement of TAVI practices in Tunisia and beyond
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None