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Efficacy of Simple Continuous Positive Airway Pressure on Patients With Obstructive Sleep Apnea

Primary Purpose

Sleep Apnea, Obstructive, Continuous Positive Airway Pressure, Polysomnography

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Simple CPAP+Conventional fixed CPAP
Simple CPAP + Auto CPAP
Sponsored by
State Key Laboratory of Respiratory Disease
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep Apnea, Obstructive

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Willing to participate after informed consent
  2. Males and females, any race and aged≥18yeras
  3. Objectively confirmed OSA with an apnoea-hypopnoea- index (AHI)≥5/h by overnight polysomnography

Exclusion Criteria:

  1. Central Sleep Apnoea/Cheyne Stokes Respiration
  2. Opioid or sedative use; Alcohol abuse
  3. Nasal congestion or tonsils more than Ⅱ degrees enlarged
  4. Optimal treatment CPAP pressure over 10cmH2O
  5. Poor understanding or being disabled

Sites / Locations

  • The First Affiliated Hospital of Guangzhou Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Conventional fixed CPAP and simple CPAP

Auto CPAP and simple CPAP

Arm Description

Participants in this group were manually titrated . They were treated with conventional fixed pressure CPAP and Simple CPAP for two separate nights in random order monitored by full polysomnography.

Participants in this group after being manually titrated were treated with Auto RemStar CPAP and Simple CPAP for two separate nights in random order monitored by full polysomnography.

Outcomes

Primary Outcome Measures

Apnea Hypopnea Index
Total number of apneas and hypopneas×60/total sleep time
Arousal Index
Total number of arousals×60/total sleep time
Oxygen Desaturation Index
Total number of oxygen desaturations≥3%×60/total sleep time
Sleep structure
Sleep stage distribution(N1, N2, N3, NREM)
Adverse effects
Using questionnaire to assess adverse effects including dyspnea, noise, bloating, et al

Secondary Outcome Measures

Full Information

First Posted
November 5, 2018
Last Updated
May 20, 2021
Sponsor
State Key Laboratory of Respiratory Disease
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1. Study Identification

Unique Protocol Identification Number
NCT03782844
Brief Title
Efficacy of Simple Continuous Positive Airway Pressure on Patients With Obstructive Sleep Apnea
Official Title
Efficacy of Simple Continuous Positive Airway Pressure on Patients With Obstructive Sleep Apnea
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
January 2, 2019 (Actual)
Primary Completion Date
October 1, 2019 (Actual)
Study Completion Date
October 15, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
State Key Laboratory of Respiratory Disease

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Obstructive sleep apnea (OSA) is a common and frequently-occurring disease. The incidence of OSA is more than 4% in general population, and as high as 20% - 40% in the elderly. At present, CPAP machines commonly used for OSA treatment includes traditional pressure fixed single-level CPAP machine and automatic pressure regulation CPAP machine. Studies have shown that the CPAP treatment pressure of OSA patients is normally below 11 cmH2O. Since the condition of OSA patients and the required CPAP treatment pressure may change over time, a CPAP machine with automatic pressure regulation function may theoretically better meet the needs of treatment. However, a recent large-scale clinical study with an average follow-up of four years showed that there was little need to change CPAP treatment pressure after titration. Although different types of CPAP have different functions, the basic principle is to keep the upper airway open and unobstructed to eliminate sleep apnea and hypopnea by continuously applying positive pressure to the upper respiratory tract through an air pump. A complex CPAP machine with functions such as pressure regulation, boost delay, end-expiratory pressure release will cost more than a single-function CPAP machine. Some patients from poor areas, even with severe OSA, may give up treatment when they can not afford CPAP machines that have not yet been included in national health insurance in China. In view of the current economic level in China, it is urgent to find an inexpensive and effective CPAP machine for the treatment of OSA and related complications. Recently, Guangzhou Yinghui Medical Technology Co., Ltd.and State Key Laboratory of Respiratory Disease have developed a new simple CPAP machine. The CPAP treatment pressure is fixed at the factory to 6 cm H2O (SKL), 8 cm H2O (SKM) and 10 cm H2O (SKH). Compared to traditional CPAP machine, only a power switch button is attached on the body, and the additional adjustment devices including display screen are removed, which not only reduces the cost of the CPAP machine, but also facilitates the operation of patients.
Detailed Description
Study Design: A randomized, cross-over and double blind study . Objective: To investigate the efficacy of simple device of continuous positive airway pressure (CPAP) in the treatment of obstructive sleep apnea (OSA). Methods: A randomized, cross-over and double blind study would be performed on 100 OSA patients using both simple CPAP and traditional CPAP during overnight polysomnography. Pressure for CPAP treatment would be manual titrated. The sleep apnea hypopnea index (AHI), arousal index (ArI), Oxygen desaturation Index (ODI), sleep structure and the preference of CPAP model were to be observed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea, Obstructive, Continuous Positive Airway Pressure, Polysomnography

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Conventional fixed CPAP and simple CPAP
Arm Type
Experimental
Arm Description
Participants in this group were manually titrated . They were treated with conventional fixed pressure CPAP and Simple CPAP for two separate nights in random order monitored by full polysomnography.
Arm Title
Auto CPAP and simple CPAP
Arm Type
Experimental
Arm Description
Participants in this group after being manually titrated were treated with Auto RemStar CPAP and Simple CPAP for two separate nights in random order monitored by full polysomnography.
Intervention Type
Device
Intervention Name(s)
Simple CPAP+Conventional fixed CPAP
Intervention Description
Patients used simple CPAP and conventional fixed CPAP during overnight polysomnography.
Intervention Type
Device
Intervention Name(s)
Simple CPAP + Auto CPAP
Intervention Description
Patients used simple CPAP and Auto CPAP during overnight polysomnography.
Primary Outcome Measure Information:
Title
Apnea Hypopnea Index
Description
Total number of apneas and hypopneas×60/total sleep time
Time Frame
One full night
Title
Arousal Index
Description
Total number of arousals×60/total sleep time
Time Frame
One full night
Title
Oxygen Desaturation Index
Description
Total number of oxygen desaturations≥3%×60/total sleep time
Time Frame
One full night
Title
Sleep structure
Description
Sleep stage distribution(N1, N2, N3, NREM)
Time Frame
One full night
Title
Adverse effects
Description
Using questionnaire to assess adverse effects including dyspnea, noise, bloating, et al
Time Frame
Onefull night

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Willing to participate after informed consent Males and females, any race and aged≥18yeras Objectively confirmed OSA with an apnoea-hypopnoea- index (AHI)≥5/h by overnight polysomnography Exclusion Criteria: Central Sleep Apnoea/Cheyne Stokes Respiration Opioid or sedative use; Alcohol abuse Nasal congestion or tonsils more than Ⅱ degrees enlarged Optimal treatment CPAP pressure over 10cmH2O Poor understanding or being disabled
Facility Information:
Facility Name
The First Affiliated Hospital of Guangzhou Medical University
City
Guangzhou
State/Province
Guangdong
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Efficacy of Simple Continuous Positive Airway Pressure on Patients With Obstructive Sleep Apnea

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