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Goal Directed Fluid Management Based on Non-invasive Monitoring

NCT01883752 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 334

Last updated 2016-02-10

No results posted yet for this study

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.

Conditions

  • Postoperative Complication

Interventions

PROCEDURE

Goal-directed Therapy group

Fluid administration is based on the respiratory variation in the pulse oximeter waveform

Sponsors & Collaborators

  • University of California, Irvine

    lead OTHER

Principal Investigators

  • Maxime Cannesson, MD, PhD · UC Irvine Medical Center, Dept of Anesthesiology & Perioperative Care

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-07-31
Primary Completion
2013-10-31
Completion
2013-10-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01883752 on ClinicalTrials.gov