NCT01191528

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Aug 2010

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2010

Completed
29 days until next milestone

First Submitted

Initial submission to the registry

August 30, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

August 31, 2010

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2010

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2010

Completed
Last Updated

December 13, 2010

Status Verified

December 1, 2010

Enrollment Period

4 months

First QC Date

August 30, 2010

Last Update Submit

December 10, 2010

Conditions

Keywords

AdultPostoperativeoximetrycapnometryIntegratedPulmonaryIndexEnd-tidalMonitoring Respiratory statuspost-operative

Interventions

Oxygen blood saturation measured by a s sensor that reflects infrared light on oxygenated and deoxygenated arterial blood via a noninvasive, clip on digit sensor connected to a combination capnometer and pulse oximeter monitor. End-tidal Carbon dioxide (EtCO2) is measured with a noninvasive nasal cannula sampling line which calculates the EtCO2 from exhaled air. Measurements recorded at 5 second intervals.

Also known as: OxiMax Nellcor, Covidien, Capnoline, Oridion Medical

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Allenmore Hospital

Tacoma, Washington, 98411, United States

Location

MeSH Terms

Conditions

Erythema Multiforme

Condition Hierarchy (Ancestors)

ErythemaSkin DiseasesSkin and Connective Tissue DiseasesSkin Diseases, Vesiculobullous

Study Officials

  • 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

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER

Study Record Dates

First Submitted

August 30, 2010

First Posted

August 31, 2010

Study Start

August 1, 2010

Primary Completion

December 1, 2010

Study Completion

December 1, 2010

Last Updated

December 13, 2010

Record last verified: 2010-12

Locations