Viewing Study NCT06627959



Ignite Creation Date: 2024-10-26 @ 3:42 PM
Last Modification Date: 2024-10-26 @ 3:42 PM
Study NCT ID: NCT06627959
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-10-01

Brief Title: StatSeal Vs Figure-of-Eight Suture for Vascular Closure in AF Ablation
Sponsor: None
Organization: None

Study Overview

Official Title: StatSeal Vs Figure-of-Eight Suture for Vascular Closure in AF Ablation
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-10
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: None
Brief Summary: This study titled aims to compare two vascular closure techniques after catheter ablation for atrial fibrillation AF Catheter ablation is a common procedure used to treat AF but after the procedure It is important to close the access site in the blood vessel to prevent bleeding This study will evaluate whether the StatSeal device a haemostatic disc can help patients recover more quickly compared to the traditional figure-of-eight suture technique

The primary objective of the study is to determine whether StatSeal reduces the time it takes for patients to start walking after the procedure known as Time to Ambulation Secondary objectives include comparing the time to complete haemostasis discharge eligibility incidence of adverse events and patient comfort between the two techniques

Participants in the study will be randomly assigned to receive either the StatSeal device or the figure-of-eight suture after their AF ablation procedure The study will recruit 160 participants across multiple hospital sites with 80 participants in each group Both techniques are standard methods and participants will be closely monitored for safety throughout the study

By comparing these two closure techniques the study aims to improve the recovery process for patients undergoing AF ablation and provide evidence on which method leads to better outcomes and patient experiences
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