A Comparison of Nursing Assessment and a Continuous Noninvasive Respiratory Volume Monitor for the Identification of Respiratory Depression and Obstructive Breathing Patterns During Phase I Anesthesia Recovery

Overview

About this study

The purpose of this study is to compare respiratory volume monitor (RVM) assessments of apnea and Low MV to nursing assessments of respiratory depressive events in patients recovering from general anesthesia during Phase I recovery.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Elective surgical patients

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Toby Weingarten, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

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CLS-20306793

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