Vascular Closure With a Device Compared to Manual Compression After Atrial Fibrillation Ablation: The LockeT II Study

NARecruitingINTERVENTIONAL
Enrollment

110

Participants

Timeline

Start Date

October 2, 2023

Primary Completion Date

December 31, 2024

Study Completion Date

December 31, 2024

Conditions
Atrial FibrillationHemostasis
Interventions
DEVICE

Vascular closure with LockeT device

For subjects that are assigned to the LockeT device arm, the healthcare professional will place the LockeT with suture above the wound to achieve compression instead of manually holding pressure on the sutures. After hemostasis is achieved and prior to ambulation the LockeT will be removed followed by suture removal.

Trial Locations (6)

64032

RECRUITING

Research Medical Center Clinic, Kansas City

RECRUITING

Research Medical Center, Kansas City

64057

RECRUITING

Centerpoint Medical Center Clinic, Independence

RECRUITING

Centerpoint Medical Center, Independence

66211

RECRUITING

Kansas City Heart Rhythm Institute - Roe Clinic, Overland Park

66215

RECRUITING

Overland Park Regional Medical Center, Overland Park

All Listed Sponsors
lead

Kansas City Heart Rhythm Research Foundation

OTHER