Evaluation of Nexfin During Anesthesia and in Intensive Care (NexfinEval)

NCT01658631 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 97

Last updated 2016-11-03

No results posted yet for this study

Summary

The purpose of this study is to compare the non invasive measurement of arterial pressure (Nexfin monitor)with the invasive measurement of arterial pressure (radial artery catheter)

* during induction of general anesthesia,
* during a leg raising test in the Intensive Care Unit

Conditions

  • Anesthesia

Interventions

DEVICE

arterial pressure measurement (Nexfin, a noninvasive finger cuff system)

Sponsors & Collaborators

  • Hopital Foch

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2015-06-30
Completion
2015-06-30

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 NCT01658631 on ClinicalTrials.gov