U.S., Feb. 18 -- ClinicalTrials.gov registry received information related to the study (NCT07414121) titled 'VASC-AF Study: Vascular Closure vs Manual Compression' on March 01, 2025.
Brief Summary: The aim of this study is to reduce the time to ambulation after PVI by a vascular closure device as compared to manual compression and a figure-of-8 suture only. Safety, efficacy and feasibility of the VASCADE MVP device should be proven, too. The definition of endpoints will be trained in all participating study sites to preserve consistency.
The primary efficacy endpoint is time to ambulation after sheath removal. Time to ambulation is defined as the elapsed time between removal of the final closure device or removal of the final sheath and w...