Effect of Non Invasive Ventilation on Lung Volumes Determined by Electrical Impedance Tomography (NIVIT)

July 30, 2015 updated by: University Hospital, Clermont-Ferrand
Effect of Non Invasive Ventilation on end-expiratory lung volumes determined by electrical impedance tomography

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

Prospective clinical study in ICU with patients requiring non invasive ventilation (NIV) comparing lung volumes determined by electrical impedance tomography before, during and after NIV.

Duration of NIV is 30 minutes.

Study Type

Observational

Enrollment (Anticipated)

20

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • France
      • Clermont-Ferrand, France, 63003
        • Recruiting
        • CHU de Clermont-Ferrand

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

patients requiring non invasive ventilation

Description

Inclusion Criteria:

  • Adult ICU patients requiring non invasive ventilation
  • Consent of patients or family
  • Arterial line

Exclusion Criteria:

  • Tracheotomized patients
  • Dressings in the thoracic area

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
non invasive ventilation (NIV)
Other: non invasive ventilation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
- End-expiratory lung volume (EELV) determined by electrical impedance tomography before, during and after NIV
Time Frame: at day 1
at day 1

Secondary Outcome Measures

Outcome Measure
Time Frame
Ventilatory frequency
Time Frame: at day 1
at day 1
Anterior, medio-anterior, medio-posterior and posterior EELV
Time Frame: at day 1
at day 1

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University Hospital, Clermont-Ferrand

Collaborators

University Hospital, Estaing

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2014

Primary Completion (Anticipated)

December 1, 2015

Study Completion (Anticipated)

December 1, 2015

Study Registration Dates

First Submitted

May 26, 2014

First Submitted That Met QC Criteria

May 28, 2014

First Posted (Estimate)

May 29, 2014

Study Record Updates

Last Update Posted (Estimate)

July 31, 2015

Last Update Submitted That Met QC Criteria

July 30, 2015

Last Verified

July 1, 2015

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • CHU-0193

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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