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

U

University Medical Center Groningen (UMCG)

Status

Completed

Conditions

Elective Hepatic Resection

Treatments

Biological: hemoglobin determination + Venofundin bolus
Biological: Hemoglobin determination + NaCl 0.9% bolus

Study type

Observational

Funder types

Other

Identifiers

NCT01060683
SpHb-001

Details and patient eligibility

About

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.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

30 participants in 2 patient groups

Group 1: 15 patients
Description:
for elective hepatic resection
Treatment:
Biological: Hemoglobin determination + NaCl 0.9% bolus
Group 2: 15
Description:
for elective hepatic resection
Treatment:
Biological: hemoglobin determination + Venofundin bolus

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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