Validation of Study in Respiratory Physiology and it Interactions (ValApPhI)

This study is currently recruiting participants.
Verified June 2013 by University Hospital, Grenoble
Sponsor:
Information provided by (Responsible Party):
University Hospital, Grenoble
ClinicalTrials.gov Identifier:
NCT01881945
First received: May 24, 2013
Last updated: June 17, 2013
Last verified: June 2013

May 24, 2013
June 17, 2013
September 2008
September 2013   (final data collection date for primary outcome measure)
  • Heart rate [ Time Frame: one measure within two weeks of inclusion ] [ Designated as safety issue: No ]
    Heart rate is calculated on electrocardiograph
  • end tidal CO2 [ Time Frame: one measure within two weeks of inclusion ] [ Designated as safety issue: No ]
    end tidal CO2 of each breath measured with an infrared CO2 analyzer
  • Non invasive arterial pressure [ Time Frame: one measure within two weeks of inclusion ] [ Designated as safety issue: No ]
  • Non invasive stroke volume [ Time Frame: one measure within two weeks of inclusion ] [ Designated as safety issue: No ]
    measured with impedance cardiography
  • Inspiratory and expiratory times [ Time Frame: one measure within two weeks of inclusion ] [ Designated as safety issue: No ]
    obtained for each breath with flow signal
  • Tidal volume [ Time Frame: one measure within two weeks of inclusion ] [ Designated as safety issue: No ]
    obtained for each breath with flow signal
Same as current
Complete list of historical versions of study NCT01881945 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Validation of Study in Respiratory Physiology and it Interactions
Validation of Tools Studying Respiratory Physiology and it Interaction With Swallowing and Cardiac Physiology.

The aim of the study was to validate tools of physiological signal processing and interpretation on healthy human volunteers in order to improve the understanding in respiratory physiology and its interactions with heart function, and swallowing.

Not Provided
Interventional
Not Provided
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Basic Science
  • Life Experiences
  • Respiratory Function
  • Cardiac Function
Other: Non-invasive physiological signal recording on healthy volunteer
Experimental: Physiological measurments
Intervention: Other: Non-invasive physiological signal recording on healthy volunteer
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
50
September 2013
September 2013   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • healthy subject
  • between 18 and 60 years old

Exclusion Criteria:

  • patient
  • person protected by the law
Both
18 Years to 60 Years
Yes
Contact: BRIOT Raphael, MCU-PH 33 4 76 63 42 86 RBriot@chu-grenoble.fr
France
 
NCT01881945
2008-A00273-52
No
University Hospital, Grenoble
University Hospital, Grenoble
Not Provided
Principal Investigator: BRIOT Raphael, MCU-PH University Hospital, Grenoble
University Hospital, Grenoble
June 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP