The Comparison of Pulse Oximetry, End-tidal Capnometry, and Integrated Pulmonary Index (IPI)

December 10, 2010 updated by: Allenmore Hospital

The Comparison of Pulse Oximetry, End-tidal Capnometry, and Integrated Pulmonary Index in Adult Post-operative Patients

To compare two ways to test breathing after surgery in acute care setting. One method tests oxygen level of the blood, and one method will test oxygen and the carbon dioxide that is breathed out.

Study Overview

Status

Completed

Conditions

Detailed Description

A simple comparison design will be used to compare pulse SpO2 monitoring of respiratory status to a combination of pulse SpO2 monitoring and EtCO2 nasal cannula monitoring with Integrated Pulmonary Index (IPI). Using combination monitor, each subject will serve as their own control with repeated measurements of respiratory rate, SpO2, EtCO2 and IPI at 5 second intervals. Patients will be monitored for a minimum of 8 hours after admission to the acute care unit and through the first night.

Subjects for this study will be a convenience sample post-operative in-patients admitted to 2 East after surgery at Allenmore Hospital/Multicare Health System a 75 bed community facility.

Study Type

Observational

Enrollment (Actual)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Washington
      • Tacoma, Washington, United States, 98411
        • Allenmore Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Convenience sample post-operative in-patients admitted to 2 East at Allenmore Hospital/multicare Health system a 75 bed community facility.

Description

Inclusion criteria:

  • Age greater than 18
  • Increased Body Mass Index (BMI) > 31
  • History of chronic obstructive pulmonary disease (COPD)
  • History of Sleep Apnea

Exclusion criteria:

  • Respiratory failure
  • Isolation requirements
  • Surgical patients admitted to 2 West or ICU

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Julie M Northrup, ADN, BC, Multicare Health System-Allenmore Hospital
  • Principal Investigator: Jennifer Spotted-Horse, MS,BSN,OCN, Multicare Health System-Allenmore Hospital
  • Principal Investigator: Dawn Fox, RN, Multicare Health System-Allenmore Hosptial
  • Principal Investigator: David Lechich, RN, Multicare Health System-Allenmore Hospital
  • Principal Investigator: Joan Fortune, RN, Multicare Health System Allenmore Hospital
  • Principal Investigator: Katy Rogers, RN, Multicare Health System, Allenmore Hospital
  • Principal Investigator: Lynn Arnold, RN, Multicare Health System Allenmore Hospital
  • Principal Investigator: Lisa Ettlin-Porter, BSN,RN,CCRN, Multicare Health System Allenmore Hospital
  • Principal Investigator: Dee Harris, BS,RRT,RPFT, Multicare Health System Allenmore Hospital
  • Principal Investigator: Colleen Doherty, PhD(c),RN, Consultant-Multicare Health System Allenmore Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2010

Primary Completion (Actual)

December 1, 2010

Study Completion (Actual)

December 1, 2010

Study Registration Dates

First Submitted

August 30, 2010

First Submitted That Met QC Criteria

August 30, 2010

First Posted (Estimate)

August 31, 2010

Study Record Updates

Last Update Posted (Estimate)

December 13, 2010

Last Update Submitted That Met QC Criteria

December 10, 2010

Last Verified

December 1, 2010

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Postoperative Care

Clinical Trials on capnostream 20, Oridian Medical 1987 ltd, Needham MA

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