← Eichor
Study identifier: NCT04005508 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

OSA and CV Outcomes in Patients With High Risk AF

Condition: Atrial Fibrillation · Obstructive Sleep Apnea  ·  Sponsor: National University of Singapore

PhaseN/A
Planned participants1365
Who can joinAll sexes, 22 Years to 99 Years
Healthy volunteersNo

About this study

The POACH study is part of the Cardiosleep research program. It is a prospective, observational, multicentre study conducted in Singapore. The recruitment target is 1365 patients. Eligible patients with AF and high cardiovascular risk will be recruited for a home-based sleep study using a FDA-approved portable device. The patients will be divided into 2 groups based on the presence or absence of OSA using apnoea-hypopnoea index ≥ 15 events/hour. The AF will be treated as per local standard practice. Participation in the POACH study will not affect the management of AF. Follow-up will be conducted every 6 months until the median follow-up duration has reached 2 years. The primary endpoint is a four-component composite of all-cause mortality, myocardial infarction, stroke and heart failure hospitalisation. Antecubital venous blood samples will be taken from the patients in the morning after the sleep study for targeted mass spectrometry which will measure 83 circulating metabolites. Sparse Principal Component Analysis will be used for data reduction. Identification of distinct associations between metabolic perturbations and OSA will be performed.

This description comes directly from the study's public registry record.

Talk to the study team

Shalini Lobo, BSc  ·  67795555  ·  shalilb@nus.edu.sg

Junping Liu, BSc  ·  67795555  ·  junping_liu@nuhs.edu.sg

Always discuss trial participation with your own doctor first.

Locations (1)

Chi-Hang LeeSingapore, SingaporeRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT04005508