Electromyographic (EMG) and Mechanomyographic (MMG) Comparison (EMG-MMG)

This study has been completed.
Sponsor:
Information provided by:
University Hospital, Grenoble
ClinicalTrials.gov Identifier:
NCT00942370
First received: July 2, 2009
Last updated: July 31, 2009
Last verified: July 2009

July 2, 2009
July 31, 2009
July 2009
July 2009   (final data collection date for primary outcome measure)
Delay between the detection by mechanomyography (MMG) of rectus abdominis contraction and the detection of cough in cough effort [ Time Frame: 2 hours ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT00942370 on ClinicalTrials.gov Archive Site
Lower and upper spectral band frequencies values for which the majority of the MMG signal is present, thresholds for detection of rectus abdominis contraction by mechanical myography [ Time Frame: 2 hours ] [ Designated as safety issue: Yes ]
Same as current
Not Provided
Not Provided
 
Electromyographic (EMG) and Mechanomyographic (MMG) Comparison
Comparison of Electromyographic With Mechanomyographic Signals of Rectus Abdominis

The purpose of this study is to assess the delay between the detection (by mechanomyography-MMG) of rectus abdominis contraction and the detection of cough in cough effort.

Not Provided
Observational
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample

Healthy volunteers

Stress Urinary Incontinence
Device: non invasive mechanomyographic device based on a 3 axes accelerometer

This biomedical research consists specifically in the simultaneous acquisition of:

  • EMG and MMG Signals of rectus abdominis of the abdomen,
  • Respiratory flow,
  • An electrocardiogram (ECG).

These acquisitions will be conducted on 16 healthy volunteers according to a standardized protocol, at rest and during voluntary cough and various physical exercises often resulting in urinary leakage in the incontinent person.

accelerometric device
Intervention: Device: non invasive mechanomyographic device based on a 3 axes accelerometer
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
16
July 2009
July 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • More or equal than 18 years old
  • Patient affiliated to social security or similarly regime
  • Healthy volunteer
  • BMI less than 30

Exclusion Criteria:

  • Pregnant women and lactating mothers
  • Ward of court or under guardianship
  • Adult unable to express their consent or person under legal protection
  • Person deprived of freedom by judicial or administrative decision
  • Person hospitalized without their consent
Both
18 Years to 65 Years
Yes
Contact information is only displayed when the study is recruiting subjects
France
 
NCT00942370
DCIC 0904
Yes
Alexandre Moreau-Gaudry, University Hospital of Grenoble
University Hospital, Grenoble
Not Provided
Principal Investigator: Alexandre Moreau-Gaudry, MD, PhD University Hospital, Grenoble
University Hospital, Grenoble
July 2009

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