UnknownNot Applicable

Comparison of Central Venous Oxygen Saturation Measurements by Non-invasive Mespere Venous Oximeter and Central Venous Catheter

Canada40 participantsStarted 2014-10

Plain-language summary

The intent of this study is to validate the venous blood oxygenation measurements of the Mespere VA Oximeter compared to the saturations measured by venous blood sampling through an inserted central vein catheter, which is currently the standard of care for measuring SvO2

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Age 18 and older * 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: * Abnormal neck anatomy * 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

What they're measuring

Mespere Venous Oximeter Accuracy Verification Study

Timeframe: up to 36 hours

Trial details

NCT IDNCT01788956

SponsorMespere Lifesciences Inc.

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2016-10

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