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The Effect of Simulated Obstructive Apnoea and Hypopnoea on Heart Rhythm in Patients With Paroxysmal Atrial Fibrillation

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Completed

Conditions

Patients With Paroxysmal Atrial Fibrillation

Treatments

Other: Inspiratory threshold
Other: Mueller manoeuvre
Other: Steady state normal breathing
Other: Expiratory apnoea

Study type

Interventional

Funder types

Other

Identifiers

NCT01796080
PAF_V1.1 (05.07.2012)

Details and patient eligibility

About

In this randomised controlled cross-over study we will investigate whether intrathoracic pressure changes induced by simulated obstructive apnoea and hypopnoea trigger premature supraventricular and ventricular contractions as well as atrial fibrillation in patients with paroxysmal atrial fibrillation.

Enrollment

45 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-75 years
  • History of ECG-documented paroxysmal atrial fibrillation within the last 12 months and currently in sinus rhythm
  • Informed consent

Exclusion criteria

  • Mental or physical disability precluding informed consent or compliance with the protocol
  • Amiodarone or Dronedarone medication
  • Previous radiofrequency ablation for atrial fibrillation
  • Severe structural heart disease

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

45 participants in 4 patient groups

Mueller manoeuvre
Active Comparator group
Description:
Mueller manoeuvre lasting for 20 seconds
Treatment:
Other: Mueller manoeuvre
Inspiratory threshold
Active Comparator group
Description:
One continuous inspiration through an inspiratory threshold load for 20 seconds
Treatment:
Other: Inspiratory threshold
Expiratory apnoea
Active Comparator group
Description:
Expiratory apnoea (without respiratory effort) lasting for 20 seconds
Treatment:
Other: Expiratory apnoea
Steady state normal breathing
Sham Comparator group
Description:
Steady state normal breathing for 20 seconds
Treatment:
Other: Steady state normal breathing

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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