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Metadata

Name
Patient Preference for Mouthpiece Ventilation
Repository
ClinicalTrials.gov
Identifier
clinicaltrials:NCT03867721
Description
BACKGROUND:

Patients with severe neuromuscular disorders (NMDs) are likely to develop progressive
respiratory insufficiency, leading to noninvasive ventilation during the night and, later,
during night and day. Ventilation via a mouthpiece (MPV) is an elegant option to offer
daytime ventilation. The patient preference regarding the ideal material for daytime MPV is
unclear.

OBJECTIVES:

The purpose of this study was to determine which ventilator, tubing support and mouthpiece
was most effective and preferred by patients with NMDs.

METHODS:

Two separate MPV equipment sets were compared in 20 patients with NMDs in a randomized
cross-over study. The first set consisted in a non-dedicated ventilator for MPV (PB560,
Covidien) combined with a customized tubing support on the shoulders and a plastic angled
mouthpiece. The second set included an MPV-dedicated ventilator (Trilogy 100, Philips
Respironics) without back-up rate and kiss trigger combined with a commercially available
tubing support and a silicone straw mouthpiece. The Borg dyspnea score, the free time without
noninvasive ventilation, the transcutaneous oxygen saturation (SpO2) and carbon dioxide
tension (TcCO2) were recorded without and with MPV. A 17-items list assessing the patient
perception about MPV sets was completed.
Data or Study Types
clinical trial
Source Organization
Unknown
Access Conditions
available
Year
2019
Access Hyperlink
https://clinicaltrials.gov/ct2/show/NCT03867721

Distributions

  • Encoding Format: HTML ; URL: https://clinicaltrials.gov/ct2/show/results/NCT03867721
This project was funded in part by grant U24AI117966 from the NIH National Institute of Allergy and Infectious Diseases as part of the Big Data to Knowledge program. We thank all members of the bioCADDIE community for their valuable input on the overall project.