Relationship Between PFTs and Pdi in DMD
Duchenne Muscular Dystrophy
About this trial
This is an interventional health services research trial for Duchenne Muscular Dystrophy
Eligibility Criteria
Inclusion Criteria:
- Clinical diagnosis of Duchenne muscular dystrophy
Exclusion Criteria:
- Inability to follow verbal instructions
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Measurement of Pdi
Measurement of SNIPs
Two small balloons, which are attached to small, flexible tubes, will be put into the esophagus (food tube) and stomach through the nose. Each balloon is about 2 inches long (deflated) and about the width of a pencil tip. A gastric balloon will be inserted into subject's stomach while an esophageal balloon will be inserted into the subject's esophagus. To reduce any discomfort with this procedure, lidocaine gel or spray will be put into the subject's nose and administered to the back of the throat before the balloon. In addition, swallowing water during the procedure will help to reduce any gagging sensation and will assure that the balloon goes into the esophagus.
While the gastric and esophageal balloon catheters are in place, the subject will be asked to perform a maximal sniff maneuver (SNIP) while one nostril is occluded with a plug containing a nasal pressure transducer to measure airway pressure during maximal inspiration. The distal end of the pressure catheter will be connected to a hand held pressure meter to display peak pressure and to provide you visual feedback. This maneuver will be performed 10 times.