CompletedNot Applicable

Non-invasive Measurement of Hemoglobin Concentration With Pulse Co-oximetry

Netherlands30 participantsStarted 2010-01

Plain-language summary

The purpose of this study is to evaluate the accuracy of continuous SpHb measurement ( Rainbow DCI, Masimo, Irvine Ca, USA) compared to the current method of monitoring (blood sampling), both during phases of hemoconcentration and hemodilution.

Who can participate

Age range18 Years

SexALL

See this in plain English?

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

Inclusion Criteria: * All patients: Age \> 18 years * ASA class I and II patient requiring hepatic resection Exclusion Criteria: * Patient refusal * Patients with a perioperative blood loss exceeding 5ml/kg

What they're measuring

To evaluate the accuracy of continuous SpHb measurement during hepatic resection compared with standard (invasive) Hb measurement

Timeframe: during operation

Trial details

NCT IDNCT01060683

SponsorUniversity Medical Center Groningen

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2011-07

View on ClinicalTrials.gov More Elective Hepatic Resection trials