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Validation of Nicom Device to Measure Stoke Volume Variation

NCT02485457 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2

Last updated 2018-01-29

No results posted yet for this study

Summary

The purpose of this study is to evaluate the ability of NICOM (Noninvasive cardiac output monitor) to detect stroke volume variation induced by leg raising or fluid expansion during surgery

Conditions

  • Anesthesia

Interventions

PROCEDURE

Volume loading

Volume loading with Ringer Lactate

DRUG

Ringer solution

Sponsors & Collaborators

  • Hopital Foch

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-28
Primary Completion
2017-06-12
Completion
2017-06-12

Countries

  • France

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 NCT02485457 on ClinicalTrials.gov