NCT02919930

Interface Selection for Adaptive Servo Ventilation

Interface Selection for Adaptive Servo Ventilation: A Randomized Controlled Study

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 15 (estimated)
• Sponsor: Universitaire Ziekenhuizen KU Leuven · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to compare the effects of nasal and oronasal interfaces during ASV treatment on sleep efficiency and sleep architecture. Therefore, patients starting treatment with ASV, will be randomized between two groups. In the first group, patients will use a nasal interface during the first night and an oronasal interface during the second night. In the second group, patients will use an oronasal mask first and a nasal mask during the second night. The results of this trial will have major impact on future clinical practice as it would deliver prediction rules to choose the correct interface immediately.

Conditions

• Central Sleep Apnea
• ASV

Interventions

Type	Name	Description
DEVICE	Switch from oronasal to nasal mask during ASV treatment	One night of ASV treatment with oronasal mask followed by one night of ASV treatment with nasal mask.
DEVICE	Switch from nasal to oronasal mask during ASV treatment	One night of ASV treatment with nasal mask followed by one night of ASV treatment with oronasal mask.

Timeline

• Start date: 2015-02-01
• Primary completion: 2025-01-01
• Completion: 2025-01-01
• First posted: 2016-09-30
• Last updated: 2024-07-03

Locations

1 site across 1 country: Belgium