Clinical Trials Directory

Trials / Completed

CompletedNCT03523013

The Outcome of CPAP Titration Under Sleep Endoscopy

The Outcome of CPAP Titration Under Sleep Endoscopy: A Randomized Controlled Crossover Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Chang Gung Memorial Hospital · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The outcome of CPAP titration under sleep endoscopy: A randomized controlled crossover trial

Detailed description

This is the study entitled "The outcome of CPAP titration under sleep endoscopy: A randomized controlled crossover trial". CPAP is first line golden standard treatment for Obstructive sleep apnea (OSA). However, the overall CPAP compliance is about 50%. One of the reasons responsible for the poor compliance is the inadequate pressure setting initially. Therefore, it is crucial for us to find out the adequate pressure as soon as possible. Sleep endoscopy is the way to evaluate upper airway obstruction of OSA patients. Meanwhile, the investigators used CPAP to titrate the adequate pressure to keep upper airway open under sleep endoscopy guidance. While the investigators find out this adequate pressure, the investigators set this pressure into CPAP program, which OSA patient will use for 1 month. To compare the different effect of CPAP under either auto-CPAP titration pressure or sleep endoscopy guidance pressure, those OSA patients will use auto-titration CPAP for 1 month as well. Another highlight of this study is the sedative agent-dexmedetomidine. Dexmedetomidine is a α2 antogonist, which cause patients sedative but less respiratory drive suppression. The mechanism of dexmedetomidine is more physiological for nature sleep.

Conditions

Interventions

TypeNameDescription
DEVICECPAPCPAP treatment with different pressure for OSA patients

Timeline

Start date
2018-02-01
Primary completion
2019-12-31
Completion
2019-12-31
First posted
2018-05-14
Last updated
2020-09-30

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT03523013. Inclusion in this directory is not an endorsement.