Non-invasive Measurement of Hemoglobin Concentration With Pulse Co-oximetry
Completed
- Conditions
- Elective Hepatic Resection
- Interventions
- Biological: Hemoglobin determination + NaCl 0.9% bolusBiological: hemoglobin determination + Venofundin bolus
- Registration Number
- NCT01060683
- Lead Sponsor
- University Medical Center Groningen
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
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
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Group 1: 15 patients Hemoglobin determination + NaCl 0.9% bolus for elective hepatic resection Group 2: 15 hemoglobin determination + Venofundin bolus for elective hepatic resection
- Primary Outcome Measures
Name Time Method To evaluate the accuracy of continuous SpHb measurement during hepatic resection compared with standard (invasive) Hb measurement during operation
- Secondary Outcome Measures
Name Time Method the effect of a bolus of crystalloid on SpHb level will be compared to the effect of a bolus of colloid on the SpHb level. during operation
Trial Locations
- Locations (1)
University Medical Center Groningen,University of Groningen, the Netherlands
🇳🇱Groningen, Netherlands
University Medical Center Groningen,University of Groningen, the Netherlands🇳🇱Groningen, Netherlands