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Clinical Trial Summary

There was no evidence to suggest that a shortened fluid fast results in an increased risk of aspiration, regurgitation or related morbidity compared with the standard 'nil by mouth from midnight' fasting policy. However, there is no available data regarding the safety and efficacy of fasting approach in patients undergoing cardiac implantable electronic device (CIED) procedures. The aim of this study is to demonstrate that a non-fasting protocol is non-inferior in regard to safety to a fasting protocol (current practice) in patients undergoing cardiac device implantation procedures


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Cardiac Implantable Electronic Devices

NCT number NCT04389697
Study type Interventional
Source Leipzig Heart Institute GmbH
Contact
Status Completed
Phase N/A
Start date January 29, 2020
Completion date December 6, 2020

See also
  Status Clinical Trial Phase
Completed NCT05361759 - National Tunisian Registry of Cardiac Implantable Electronic Devices