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

NCT ID: NCT06138626

Last Updated: 2025-07-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

336 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-11-15

Study Completion Date

2024-12-23

Brief Summary

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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.

Detailed Description

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Conditions

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Anesthesia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Alert active

Anesthesia provider will see alert when fresh gas flow is excessive

Group Type EXPERIMENTAL

Alert

Intervention Type BEHAVIORAL

An alert that appears when anesthetic fresh gas flow is excessive

Alert inactive

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

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Alert

An alert that appears when anesthetic fresh gas flow is excessive

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Anesthesia provider using electronic medical record at study site

Exclusion Criteria

* None
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Stanford University

OTHER

Sponsor Role lead

Responsible Party

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Daniel Gessner

Clinical Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Stanford University

Palo Alto, California, United States

Site Status

Countries

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United States

Other Identifiers

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63548

Identifier Type: -

Identifier Source: org_study_id

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