Goal Directed Fluid Management Based on Non-invasive Monitoring
Status: | Completed |
---|---|
Conditions: | Hospital |
Therapuetic Areas: | Other |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | July 2011 |
End Date: | October 2013 |
Goal-Directed Fluid Management Based on Non- Invasive Monitoring of Pulse Oximeter-Derived Pleth Variability Index
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.
respiratory variations in the oxygen saturation by pulse oximetry (SpO2) waveform has
potential to decrease postoperative complications and outcomes.
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.
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.
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
We found this trial at
1
site
101 The City Drive South
Orange, California 92868
Orange, California 92868
714-456-7890
University of California, Irvine Medical Center We are UC Irvine Health. We are a devoted...
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