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NCT06138626 Clinical Trial

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

Anesthesia Clinical Trial

Official title:
Anesthetic Fresh Gas Flow Alert Test

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT06138626
Other study ID # 63548
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date November 15, 2023
Est. completion date November 15, 2024

Study information
Verified date November 2023
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 300
Est. completion date November 15, 2024
Est. primary completion date November 15, 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Anesthesia provider using electronic medical record at study site Exclusion Criteria: - None

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Alert
An alert that appears when anesthetic fresh gas flow is excessive

Locations
Country Name City State
United States Stanford University Palo Alto California

Sponsors (1)
Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary 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
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