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OpenTrials
Completed

NCT Number: NCT01658631

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

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

Completed

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Institut Mutualiste Montsouris, Paris, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age >18
  • ASA II, III or IV
  • weight between 40 and 180 kg; BMI < 35
  • normal Allen's test and/or hand Doppler examination.

Exclusion criteria

  • cardiac arrhythmias,
  • history of vascular surgery or vascular implant in the upper limb
  • Raynaud disease

Treatment and study plan

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

Device

Primary outcomes

  1. Arterial pressure measurement

    Time frame: Blood pressure will be followed for the duration of induction of anesthesia, an expected average of 20 minutes, or for the passive legs raising test, an expected average of 20 minutes

Sponsors and collaborators

Lead sponsor

Hopital Foch

Other

Registry information

Official study title

Evaluation of Nexfin During Induction of General Anesthesia and in Intensive Care During a Passive Legs Raising Test

Important dates

Study start
2012
Primary completion
2015
Study completion
2015
First posted
Aug 7, 2012
Registry last updated
Nov 3, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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