NCT04079543 (FAST) is a NA clinical trial of NPO past midnight in Patient Satisfaction, sponsored by Stony Brook University.

Who is sponsoring NCT04079543?

NCT04079543 is sponsored by Stony Brook University.

What drugs are being tested in NCT04079543?

Interventions in NCT04079543: NPO past midnight, NPO.

What condition does NCT04079543 study?

NCT04079543 studies Patient Satisfaction, Dehydration, Physiological Effects Secondary to Dehydration.

Is NCT04079543 still recruiting?

NCT04079543 is currently status unknown. Last updated 6 September 2019.

Last reviewed 2019-09-06 · How we verify

NCT04079543: FAST

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

NPO and Patient Satisfaction in the Cath Lab

Status unknown NA Last updated 6 September 2019

What this trial tests

NA trial testing NPO past midnight in Patient Satisfaction in 200 participants. Status unknown.

Timeline

9 September 2019

Primary endpoint
9 September 2020

9 September 2021

Quick facts

Lead sponsor	Stony Brook University
Phase	NA
Status	Status unknown
Study type	INTERVENTIONAL
Allocation	randomized
Design	parallel
Masking	none
Primary purpose	treatment
Enrollment	200
Start date	9 September 2019
Primary completion	9 September 2020
Estimated completion	9 September 2021

Drugs / interventions tested

NPO past midnight
NPO

Conditions studied

Patient Satisfaction — all drugs for Patient Satisfaction →
Dehydration — all drugs for Dehydration →
Physiological Effects Secondary to Dehydration — all drugs for Physiological Effects Secondary to Dehydration →

Sponsor

Stony Brook University

Who can join

18 and older, any sex, with Patient Satisfaction or Dehydration. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

Randomized controlled trial of liberal vs. standard fasting instructions in percutaneous cardiac procedures.
Atkinson DJ, Romeiser JL, Almasry IO, Tannous HJ, et al · · 2023 · cited 11× · PMID 37553699 · DOI 10.1186/s13741-023-00333-z

Verify or expand the search:

Other recruiting trials for Patient Satisfaction

Currently open trials in the same condition.

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Other Stony Brook University trials

Trials by the same sponsor.

NCT07478250 — First Responder Safety Training (FiRST) · NA · not yet recruiting
NCT07076342 — The Role of mGluR5 in CBT-I · Phase 4 · recruiting
NCT07009691 — Hydrogen Water Intervention With Heart Rate Variability as an Outcome Biomarker in ME/CFS · NA · recruiting
NCT07114900 — Randomized Controlled Physical Activity App Intervention for Black Women · Phase 3 · active not recruiting
NCT05245227 — Double Simultaneous Uterotonic Agents Versus Single Agent Regimen to Prevent Early Postpartum Hemorrhage · Phase 3 · recruiting

Verify against primary sources

ClinicalTrials.gov — authoritative US registry record
WHO ICTRP — international registry index
EU Clinical Trials Register
Sponsor press releases (Google)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT04079543 (US National Library of Medicine, public domain)
Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Stony Brook University
Last refreshed: 6 September 2019

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04079543.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing