Value of Screening and Treatment of SAHS in the Management of AF Ablation Candidates

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHospital San Carlos, Madrid

About this trial

The present prospective cohort study (not randomized) analyses the value of screening and treatment of SAHS in the management of patients with AF refractory to antiarrhythmics drugs, potentially candidates for ablation.

Patients at low risk of suffering from SAHS will follow conventional management of their AF, according to the usual criteria of the Arrhythmia Unit. Patients with high or intermediate risk of SAHS, will undergo respiratory polygraphy. If the result is positive, they will be treated as standard for this syndrome and their heart rate will be monitored for 3 months. After this, the patient's arrhythmic load will be reevaluated differentiating patients into two groups, those that must be ablated from those that have improved their condition and the clinical criteria is no longer ablation but follow-up.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with paroxysmal or persistent atrial fibrillation

Recurrent atrial fibrillation despite treatment with at least one class I or III antiarrhythmic

No previous diagnosis of apnea-hypopnea syndrome

Disqualifiers

Patients <18 years

Pregnant women

Doubts about the patient's ability to perform a home respiratory polygraphy

Doubts about the patient's ability to acquire rhythm records with the Kardia system (smartphone required)

Trial design

Design model

Sequential

Treatments tested in this trial

  • Treatment of SAHS

    Other intervention

    Patients diagnosed with SAHS will be treated in the Pneumology Service according to usual practice (dietary hygienic measures, CPAP, etc.).

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Patients with negative diagnosis of SAHSNo intervention 0 interventions
Group B: Patients with positive diagnosis of SAHSOther 1 intervention

Trial outcomes

Primary outcomes

1

Arrhythmic load

Rate of time in FA measured with Kardia © recorder

Time frame
Six months

Secondary outcomes

Other outcomes

Sponsors and contacts

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