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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03242720
Other study ID # 41798
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date January 1, 2019
Est. completion date December 2020

Study information

Verified date May 2022
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

With this pilot study, we are hoping to test the feasibility of a larger study in the future and to learn whether positive airway pressure therapy reduces the recurrence risk of atrial fibrillation after successful catheter ablation procedure among patients with atrial fibrillation and obstructive sleep apnea. The results from this study will help us refine the design for a future larger study, and will ultimately improve care of patients with obstructive sleep apnea and atrial fibrillation.


Description:

Obstructive sleep apnea, a sleep-related breathing disorder in which breathing stops for short periods during sleep, is a common condition in patients with atrial fibrillation. Studies have shown that up to 75% of atrial fibrillation patients undergoing catheter ablation procedure have obstructive sleep apnea. Obstructive sleep apnea increases the risk of atrial fibrillation recurrence after successful catheter ablation by 40%. However, whether treatment of obstructive sleep apnea with positive airway pressure (PAP, the current most effective treatment for obstructive sleep apnea that uses a machine to help breathe more easily) reduces the risk of atrial fibrillation recurrence is not fully understood. The purpose of this study, therefore, is to examine whether positive airway pressure therapy reduces atrial fibrillation recurrence after catheter ablation in patients with obstructive sleep apnea and atrial fibrillation.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2020
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Men and women 18 years or older 2. First-time catheter ablation for atrial fibrillation 3. Moderate-to-severe obstructive sleep apnea diagnosed with a sleep study (apnea-hypopnea index = 15) Exclusion Criteria: 1. Current or prior use of positive airway pressure for obstructive sleep apnea 2. Any household member with current/past positive airway pressure use 3. Did not meet minimal adherence to positive airway pressure treatment (= 4 hours/night and = 70% of time in 2 weeks) 4. History of motor vehicle or occupational accident related to excessive sleepiness 5. Severe nocturnal desaturation documented on sleep study as >10% of total sleep time with oxygen saturation of < 75% 6. Any condition determined by physicians that constrains the use of positive airway pressure such as anatomically fixed nasal obstruction, neurological impairment, and significant claustrophobia. 7. Congestive heart failure (New York Heart Association IV) 8. Severe valvular disease 9. Planned coronary revascularization procedure in the next 6 months 10. Severe pulmonary disease 11. Participation in another treatment intervention trial that might influence results of this trial 12. Ablation procedure scheduled in the next 8 weeks

Study Design


Intervention

Procedure:
Cardiac Ablation for Atrial Fibrillation
Ablation of arrhythmia focus in the heart for atrial fibrillation

Locations

Country Name City State
United States Stanford Sleep Medicine Center Redwood City California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Atrial Fibrillation recurrence Risk of Atrial Fibrillation recurrence 6 months after ablation
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