NCT06138626

Brief Summary

The primary objective of this quality improvement intervention is to test the efficacy of excessive fresh gas flow alerting in the electronic medical record for anesthesia providers.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
336

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 9, 2023

Completed
6 days until next milestone

Study Start

First participant enrolled

November 15, 2023

Completed
3 days until next milestone

First Posted

Study publicly available on registry

November 18, 2023

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 19, 2024

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 23, 2024

Completed
Last Updated

April 23, 2026

Status Verified

April 1, 2026

Enrollment Period

7 months

First QC Date

November 9, 2023

Last Update Submit

April 21, 2026

Conditions

Anesthesia

Outcome Measures

Primary Outcomes (1)

  • Mean change in average fresh gas flow from baseline at 90 days

    Mean change in average total fresh gas flow, in liters per minute as recorded in the electronic medical record, when administering sevoflurane, averaged over 1 week at baseline and over 1 week at 90 days

    Baseline, day 90

Study Arms (2)

Alert active

EXPERIMENTAL

Anesthesia provider will see alert when fresh gas flow is excessive

Behavioral: Alert

Alert inactive

NO INTERVENTION

Anesthesia provider will not see alert when fresh gas flow is excessive

Interventions

AlertBEHAVIORAL

An alert that appears when anesthetic fresh gas flow is excessive

Alert active

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Anesthesia provider using electronic medical record at study site

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Stanford University

Palo Alto, California, 94305, United States

Location

MeSH Terms

Interventions

Caffeine

Intervention Hierarchy (Ancestors)

XanthinesAlkaloidsHeterocyclic CompoundsPurinonesPurinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-Ring

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Assistant Professor

Study Record Dates

First Submitted

November 9, 2023

First Posted

November 18, 2023

Study Start

November 15, 2023

Primary Completion

June 19, 2024

Study Completion

December 23, 2024

Last Updated

April 23, 2026

Record last verified: 2026-04

Locations

US(1)