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NCT04947397 Clinical Trial

Investigation of Pupillometry as Guide for Extubation Readiness in Anesthetized Children

Anesthesia Clinical Trial

Official title:
Investigation of Pupillometry as Guide for Extubation Readiness in Anesthetized Children

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04947397
Other study ID # 20-32664
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 20, 2022
Est. completion date December 31, 2023

Study information
Verified date December 2023
Source University of California, San Francisco
Contact Daniel Abelson, MD
Phone (510) 428-3070
Email daniel.abelson@ucsf.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Investigation of pupillometry as guide for extubation readiness in anesthetized children.

Description:

Can a pupil metric be used to make extubation more safe in anesthetized children?

Recruitment information / eligibility
Status Recruiting
Enrollment 20
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 2 Years to 10 Years
Eligibility Inclusion Criteria: - Children undergoing general anesthesia and endotracheal intubation for surgery. - American Society of Anesthesiologists Physical Status Class I and II patients. Exclusion Criteria: - Central nervous system abnormality. - Ophthalmologic abnormality.

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Pupillometry
Pupillometry prior to extubation

Locations
Country Name City State
United States UCSF Benioff Children's Hospital Oakland Oakland California

Sponsors (1)
Lead Sponsor Collaborator
University of California, San Francisco

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Other Breath-holding Measurement tool: Capnogram Prior to extubation
Primary Extubation success Extubation without pathologic airway response such as laryngospasm Immediately after extubation
Secondary Anesthetic vapor concentration at extubation At the time of extubation
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