Comparison of Central Venous Oxygen Saturation Measurements by Non-invasive Mespere Venous Oximeter and Central Venous Catheter
NCT ID: NCT01788956
Last Updated: 2015-09-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
40 participants
OBSERVATIONAL
2014-10-31
2016-10-31
Brief Summary
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Detailed Description
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The existing method for venous blood oxygenation monitored is either through an invasive fiber optic catheter, or intermittently by blood sampling through a central venous catheter Oximetry. However, SvO2 measurements using fiber optic catheters are very expensive, and all central line insertions include inherent risks. Also, insertion of a central line is in some circumstances not feasible (e.g. discomfort/limited experience in central line insertion, unavailability of specific monitoring systems etc.) resulting in inappropriate therapy usually guided by SvO2. Therefore, a non-invasive monitor to measure SvO2 at the bedside negating the requirement for a central line insertion would be of clinical benefit and allow appropriate therapy of many patients listed above at a time when therapy has the most benefit.
The Mespere VA Oximeter is a non-invasive medical device for monitoring of venous blood oxygenation.
Continuous measurement of venous oxygenation will be beneficial because it will help the physician better understand local ischemia as well as provide better guidance for the physician to be able to best treat the patient and decrease their burden of illness.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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ICU Patients
80 subjects (male and female)
Mespere Venous Oximeter
Mespere Venous oximeter provides non-invasive measurement of the oxygenation of the venous blood.
Co-Oximeter
Interventions
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Mespere Venous Oximeter
Mespere Venous oximeter provides non-invasive measurement of the oxygenation of the venous blood.
Co-Oximeter
Eligibility Criteria
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Inclusion Criteria
* Patients admitted to the ICU
* Patients who have or are scheduled to have an indwelling central venous catheter inserted via the internal jugular vein or subclavian vein as part of their usual care
Exclusion Criteria
* Unable to identify jugular vein under ultrasound guidance
* Allergic to adhesive tape
* Presence of known anatomical shunt or AV dialysis fistula
* Known central vein stenosis
18 Years
ALL
No
Sponsors
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Mespere Lifesciences Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Michael Sharpe, MD, FRCPC
Role: PRINCIPAL_INVESTIGATOR
LHSC University Hospital
Locations
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London Health Sciences Center, University Hospital
London, Ontario, Canada
Countries
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Other Identifiers
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MLS STP-9100002
Identifier Type: -
Identifier Source: org_study_id
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