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

  • Study type

    Observational
  • Study IDs

  • Describes the nature of a clinical study. Types include:

    • Observational study — observes people and measures outcomes without affecting results.
    • Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
    • Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
  • Site IRB
    • Rochester, Minnesota: 15-005133
    Sponsor Protocol Number: 15-005133

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. If you need assistance understanding the eligibility criteria, please contact the study team.

See eligibility criteria

Inclusion Criteria:

  • Elective surgical patients

Participating Mayo Clinic locations

Study statuses change often. Please contact us for help.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Toby Weingarten, M.D.

Closed for enrollment

Contact information:

Shonie Buenvenida R.N.

(507)255-8248

buenvenida.shonie@mayo.edu