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Electromyographic (EMG) and Mechanomyographic (MMG) Comparison

Completed
Conditions
Stress Urinary Incontinence
Interventions
Device: non invasive mechanomyographic device based on a 3 axes accelerometer
Registration Number
NCT00942370
Lead Sponsor
University Hospital, Grenoble
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
16
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

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
accelerometric devicenon invasive mechanomyographic device based on a 3 axes accelerometer-
Primary Outcome Measures
NameTimeMethod
Delay between the detection by mechanomyography (MMG) of rectus abdominis contraction and the detection of cough in cough effort2 hours
Secondary Outcome Measures
NameTimeMethod
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 myography2 hours

Trial Locations

Locations (1)

Clinical Investigation Center - INSERM - University Hospital of Grenoble

🇫🇷

Grenoble, France

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