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Test of Excessive Anesthetic Fresh Gas Flow Alerting in the Electronic Medical Record to Reduce Excessive Fresh Gas Flow

Anesthetic Fresh Gas Flow Alert Test

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06138626
Enrollment
336
Registered
2023-11-18
Start date
2023-11-15
Completion date
2024-12-23
Last updated
2026-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia

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.

Interventions

BEHAVIORALAlert

An alert that appears when anesthetic fresh gas flow is excessive

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Anesthesia provider using electronic medical record at study site

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Mean change in average fresh gas flow from baseline at 90 daysBaseline, day 90Mean 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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 24, 2026