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Clinical Trial Summary

The purpose of this randomized, control study is to compare liberal vs strict nil per os (NPO) policies on patients undergoing transcatheter aortic valve replacement (TAVR) or arrhythmia ablation. The primary objective of this study is to determine if allowing clear liquids up to 2 hours prior to elective TAVR or elective arrhythmia ablation procedure improves patient satisfaction.


Clinical Trial Description

After informed written consent, patients will be randomized into one of the two groups: Strict NPO (NPO after midnight) or liberal NPO (clear liquids up to 2 hours prior to procedure). All patients, regardless of study arm, will be allowed to take medications with a sip of water. All other peri-operative care will be routine. On the day of the procedure, a patient satisfaction survey will be completed and the procedure will be performed as routine. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04079543
Study type Interventional
Source Stony Brook University
Contact Derek Atkinson, MD
Phone 631-748-9310
Email derek.atkinson@stonybrookmedicine.edu
Status Not yet recruiting
Phase N/A
Start date September 9, 2019
Completion date September 9, 2021

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