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NPO and Patient Satisfaction in the Cath Lab

NCT04079543 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2019-09-06

No results posted yet for this study

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.

Conditions

  • Patient Satisfaction
  • Dehydration
  • Physiological Effects Secondary to Dehydration

Interventions

OTHER

NPO past midnight

NPO after midnight (solids and liquids), except for a sip of water with medication.

OTHER

NPO

No solids after midnight. Clear liquids up to 2 hours prior to procedure. Patients can take medications with a sip of water.

Sponsors & Collaborators

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-09
Primary Completion
2020-09-09
Completion
2021-09-09

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04079543 on ClinicalTrials.gov