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Clinical Trials/NCT01883752
NCT01883752
Completed
Not Applicable

Goal-Directed Fluid Management Based on Non- Invasive Monitoring of Pulse Oximeter-Derived Pleth Variability Index

University of California, Irvine1 site in 1 country334 target enrollmentJuly 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Complication
Sponsor
University of California, Irvine
Enrollment
334
Locations
1
Primary Endpoint
Duration of hospital stay
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to evaluate whether goal directed fluid management using respiratory variations in the oxygen saturation by pulse oximetry (SpO2) waveform has potential to decrease postoperative complications and outcomes.

Detailed Description

The aim of this study is to test the hypothesis that monitoring and minimizing the respiratory variations in the pulse oximeter waveform amplitude by volume loading has potential to decrease postoperative morbidity and length of stay in the hospital in patients undergoing routine, moderate-risk elective surgery. In this study the investigators will test the impact of hemodynamic optimization based on the respiratory variations in the plethysmographic waveform amplitude to decrease postoperative morbidity and length of stay in the hospital in patients undergoing routine, moderate-risk elective surgery. The primary outcome variable is the incidence of postoperative complications. Secondary outcome variables are the duration of hospital and ICU stays, postoperative mortality, and cost of surgery.

Registry
clinicaltrials.gov
Start Date
July 2011
End Date
October 2013
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Maxime Cannesson

Associate Professor

University of California, Irvine

Eligibility Criteria

Inclusion Criteria

  • Patients (male or female)
  • Over 18 years old undergoing non-cardiac surgery
  • Weight \> 40 kg, Body Mass Index \< 40

Exclusion Criteria

  • Patients who do not consent
  • Body Mass Index \> 40

Outcomes

Primary Outcomes

Duration of hospital stay

Time Frame: Maximum 90 days after surgery

The length of stay in the hospital is defined as postoperative number of days in the hospital until discharge.

Study Sites (1)

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