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Regional Distribution of Ventilation to Assess Respiratory Muscle Dysfunction

Construction of a Database to Identify Early Indicators of Respiratory Muscle Dysfunction in Neuromuscular Patients From the Optoelectronic Plethysmography Assessment of the Thoracoabdominal Motion

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01569217
Acronym
DREM
Enrollment
200
Registered
2012-04-03
Start date
2011-06-30
Completion date
2018-07-31
Last updated
2017-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diaphragmatic Paralysis, Neuromuscular Disorder, Respiratory Failure

Keywords

Diaphragm, Abdomen, Breathing pattern, dyspnea

Brief summary

The aim of this study is to better discriminate respiratory muscle dysfunction by comparing the measurements of thoracoabdominal motion obtained by an optoelectronic recording and the conventional tests of respiratory muscle strength. The final objective is to better select in the future the patients who need more specific assessment of diaphragmatic function like maximal transdiaphragmatic pressure measurement and phrenic nerve stimulation.

Detailed description

All patients which had suspected respiratory muscle dysfunction will have usual exploration of the respiratory muscles according to the clinician prescription. These explorations can include : * Lung volumes in seating and supine position * Maximal inspiratory and expiratory pressures * Maximal sniff pressures And when diaphragmatic dysfunction is suspected : * Maximal transdiaphragmatic pressure * Phrenic nerve conduction These patients will also beneficiate to the determination of volume variations of the upper rib cage, the lower rib cage and the abdominal compartments by using Opto-electronic plethysmography.

Interventions

None listed

Sponsors

Centre d'Investigation Clinique et Technologique 805
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* suspicion of respiratory muscle dysfunction * indication of diaphragm exploration

Exclusion criteria

* acute respiratory failure

Design outcomes

Primary

MeasureTime frameDescription
compartmental distribution of the inspired/expired volumes1 hourMeasurements of the thoraco-abdominal motion and of the global lung volume changes. Measurements will be done during spontaneous breathing and during vital capacity maneuvers. Therefore the tidal volume, the inspiratory capacity and the expiratory reserve volume will be measured in liters and for each compartiment (upper thorax, lower thorax, abdomen) contribution of these volumes will be expressed in percentage.

Secondary

MeasureTime frameDescription
left side and right side contribution to the inspired/expired volumes1 hourMeasurements will be done during spontaneous breathing and during vital capacity maneuvers. Therefore the tidal volume, the inspiratory capacity and the expiratory reserve volume will be measured in liters and each side contribution of these volumes will be expressed in percentage.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026