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Trial record 27 of 2402 for:    CARBON DIOXIDE

Comparison of End-tidal Carbon Dioxide (ETCO2) Measured by Transportable Capnometer (EMMATM) and the Arterial pCO2 in General Anesthesia

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ClinicalTrials.gov Identifier: NCT02184728
Recruitment Status : Completed
First Posted : July 9, 2014
Last Update Posted : March 25, 2015
Sponsor:
Information provided by (Responsible Party):
Sira Bang, Inje University

Brief Summary:
An end-tidal CO 2 monitor (capnometer) is used most often as a noninvasive substitute for PaCO2 in anesthesia, anesthetic recovery and intensive care. There is now also wide-spread use of capnometry on-site at emergency and trauma fields. So, portable device can be used usefully.

Condition or disease Intervention/treatment Phase
End Tidal Carbon Dioxide of Patients Undergoing General Anesthesia Device: End-tidal CO2(portable capnometer) Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 35 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Study Start Date : June 2014
Actual Primary Completion Date : January 2015
Actual Study Completion Date : March 2015

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
No Intervention: EMMA(TM)

A small capnograph for measuring ET-CO2 - the EMMA capnometer

1

Device: End-tidal CO2(portable capnometer)
End-tidal CO2(portable capnometer: EMMATM, Side stream capnometry module:Datex-Ohmeda S5 Anesthesia Monitor )levels were recorded at the time of arterial blood gas sampling.
Other Name: EMMA(TM )




Primary Outcome Measures :
  1. End-tidal CO2 [ Time Frame: During operation (2-4 times) ]
    End-tidal CO2(portable capnometer: EMMATM, Side stream capnometry module:Datex-Ohmeda S5 Anesthesia Monitor )levels were recorded at the time of arterial blood gas sampling.



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Ages Eligible for Study:   20 Years to 85 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • patients who anticipated arterial gas analyze intraoperatively

Exclusion Criteria:

  • patients who didn't get arterial line

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02184728


Locations
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Korea, Republic of
Inje University Seoul Paik Hospital, Seoul, Korea
Seoul, Jung-Gu,, Korea, Republic of, 100-032
Sponsors and Collaborators
Inje University

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Sira Bang, Assistant Professor, Inje University
ClinicalTrials.gov Identifier: NCT02184728     History of Changes
Other Study ID Numbers: IIT-2014-215
First Posted: July 9, 2014    Key Record Dates
Last Update Posted: March 25, 2015
Last Verified: March 2015

Keywords provided by Sira Bang, Inje University:
end-tidal CO2
capnometer