CPAP in AF Patients With OSA (CPAPAF)
Primary Purpose
Atrial Fibrillation, Sleep Apnea
Status
Recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
continuous positive airway pressure
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Atrial Fibrillation focused on measuring Atrial Fibrillation, sleep apnea
Eligibility Criteria
Inclusion Criteria:
- men or women aged 20 to 65 years
- paroxysmal AF, diagnosed based on the ACC/AHA/HRS 2014 guideline, and is defined as AF that terminates spontaneously or with intervention within 7 d of onset either by 12-lead EKG, 24-hr Holter, or 14-day ECG monitor.
- OSA, defined as an AHI>15/hr of sleep, of which >50% of events are obstructive.
- Informed consent signed
Exclusion Criteria:
- Moderate-severe valvular heart diseases (regurgitation or stenosis)
- post heart surgery
- Uncontrolled systemic hypertension or pulmonary hypertension
- Use of psychoactive or other drugs that could influence breathing patterns
- Current use of CPAP treatment
- Epworth sleepiness scale>10
- Congestive heart failure (LVEF≦45%)
- Chronic obstructive pulmonary disease
- History of stroke or neuromuscular disease
- Severe insomnia
Sites / Locations
- National Taiwan University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
CPAP treatment for 12 months
Placebo
Arm Description
CPAP treatment for 12 months
observation
Outcomes
Primary Outcome Measures
Change of AF burden
The duration in AF on 14-day ECG monitor (percent)
change of left atrium volume
LA volume index measured by ultrasonocardiography
change of Quality of Life
Questionnaire (Short Form Health Survey-36); higher scores means a better quality of life; maximal score 100%
Number of participants hospitalized for cardiovascular or all causes
Hospitalization for cardiovascular or all causes within the follow-up period
Secondary Outcome Measures
Full Information
NCT ID
NCT04513483
First Posted
August 6, 2020
Last Updated
April 25, 2023
Sponsor
National Taiwan University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04513483
Brief Title
CPAP in AF Patients With OSA
Acronym
CPAPAF
Official Title
The Effect of Continuous Positive Airway Pressure in Patients With Obstructive Sleep Apnea and Paroxysmal Atrial Fibrillation
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 7, 2020 (Actual)
Primary Completion Date
December 31, 2026 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Obstructive sleep apnea is associated with atrial fibrillation. This study is to evaluate the effect of continuous positive airway pressure on the burden of atrial fibrillation in the patients with obstructive sleep apnea and paroxysmal atrial fibrillation.
Detailed Description
Traditional risk factors for AF were established from the original Framingham Heart Study cohort which showed aging, hypertension, congestive heart failure, coronary artery disease, valvular heart disease and diabetes mellitus (DM) as independent risk factors. In the past decade, several important risk factors not encompassed in previous studies have also been found to have a link with AF. One of these newly-identified risk factors is obstructive sleep apnea (OSA), which has been listed as one of the risk factor needed to be assessed and treated in AF patients.
OSA and AF often co-exist and indeed share some risk factors, such as hypertension. AF Patients are more likely to have OSA, with reported prevalence rates of OSA (apnea-hypopnea index [AHI] ≥15) as high as 62% in AF cohorts from hospital-based studies. In community-based cohort studies, a cross-sectional analysis from sleep heart health study (SHSS) found those with sleep-disordered breathing(SDB)/sleep apnea (SA) (respiratory disturbance index [RDI] ≥ 30) had four times the odds of a polysomnography (PSG)-detected nocturnal AF as compared to those without SDB/SA after adjusting confounders. Following from this, a cross-sectional study on Outcomes of Sleep Disorders in Older Men Study (MrOS Sleep Study) showed a dose-response association between RDI and AF.
There are several pathophysiological mechanisms by which OSA could potentially increase the risk of development of new AF, or trigger a recurrence of AF in a patient with an established history of AF. OSA is characterized by repetitive collapse of the upper airway (UA) during sleep. The UA collapses when sleep-related loss in UA dilator muscle tone is superimposed upon a narrow and/or collapsible airway. These obstructive apneas or hypopneas, characterized by unsuccessful inspiratory efforts against an occluded airway, lead to 1) exaggerated negative intrathoracic pressure swings 2) hypoxia, and 3) co-activation of sympathetic and parasympathetic systems, all of which have been shown to potentiate a pro-arrhythmic state. Given that these mechanisms are pro-arrhythmic, CPAP (continuous positive airway pressure), the gold standard therapy for OSA, works by splinting the upper airway open during sleep with subsequent abolition of swings in pressure, hypoxia and arousals, can potentially modify the risk of development of AF or recurrence of AF in OSA patients.
There is a growing body of literature supporting that OSA being as a risk factor for recurrence of AF after cardioversion or ablation and treatment of OSA with CPAP decreased the risk of recurrence of AF. Nevertheless, all of the aforementioned studies are observational or retrospective in nature. Recently, Caples et al. conducted the first randomized control trial using CPAP in patients with AF and OSA but failed to find a difference of recurrence of AF between those treated with CPAP versus usual care. Notably, there are several issues in the study design and methodology that do not allow for firm conclusion from the results of this study. It was a single-center study, enrolling very small number of patients, and used a low cut-off AHI>5/h as inclusion criteria. More importantly, only patients with persistent AF scheduled for cardioversion were included. Given the natural time-course from paroxysmal AF to persistent AF, long-term remodeling or established atrial arrythmogenic substrate in persistent AF may be less or not reversible even when the initial risk factor is removed. In this regard, early intervention with CPAP in patients with paroxysmal AF and OSA, which has never been done in previous studies, should confer a better antiarrythmic effect. Therefore, the investigators aim to test the hypothesis that treatment of OSA with CPAP would reduce the burden of AF in patients with paroxysmal AF.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation, Sleep Apnea
Keywords
Atrial Fibrillation, sleep apnea
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
CPAP treatment for 12 months
Arm Type
Experimental
Arm Description
CPAP treatment for 12 months
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
observation
Intervention Type
Device
Intervention Name(s)
continuous positive airway pressure
Intervention Description
CPAP treatment at night. Treat AF as cardiologist's discretion.
Intervention Type
Device
Intervention Name(s)
Placebo
Intervention Description
Observation. Treat AF as cardiologist's discretion.
Primary Outcome Measure Information:
Title
Change of AF burden
Description
The duration in AF on 14-day ECG monitor (percent)
Time Frame
0, 6, 12 months
Title
change of left atrium volume
Description
LA volume index measured by ultrasonocardiography
Time Frame
0, 6, 12 months
Title
change of Quality of Life
Description
Questionnaire (Short Form Health Survey-36); higher scores means a better quality of life; maximal score 100%
Time Frame
0, 6, 12 months
Title
Number of participants hospitalized for cardiovascular or all causes
Description
Hospitalization for cardiovascular or all causes within the follow-up period
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
men or women aged 20 to 65 years
paroxysmal AF, diagnosed based on the ACC/AHA/HRS 2014 guideline, and is defined as AF that terminates spontaneously or with intervention within 7 d of onset either by 12-lead EKG, 24-hr Holter, or 14-day ECG monitor.
OSA, defined as an AHI>15/hr of sleep, of which >50% of events are obstructive.
Informed consent signed
Exclusion Criteria:
Moderate-severe valvular heart diseases (regurgitation or stenosis)
post heart surgery
Uncontrolled systemic hypertension or pulmonary hypertension
Use of psychoactive or other drugs that could influence breathing patterns
Current use of CPAP treatment
Epworth sleepiness scale>10
Congestive heart failure (LVEF≦45%)
Chronic obstructive pulmonary disease
History of stroke or neuromuscular disease
Severe insomnia
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chih-Chieh C Yu, MD.PhD
Phone
886-2-23123456
Ext
65257
Email
sweetchieh@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chih-Chieh Yu, MD.PhD
Organizational Affiliation
National Taiwan University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Taiwan University Hospital
City
Taipei
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chih-Chieh Yu, MD.PhD.
Phone
886-2-23123456
Ext
65257
Email
sweetchieh@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
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