NCT06313840Completed
Central Sleep Apnea Prevalence and Impact on Cognitive Function in Patients With Heart Failure With Reduced or Mildly Reduced Left Ventricular Ejection Fraction
Source: ClinicalTrials.gov · Last updated 10 Feb 2025
Brief summary (registry, in English)
Study to assess the prevalence of central sleep apnea in patients with heart failure with reduced or mildly reduced left ventricular ejection fraction (LVEF \<50%) followed by case-control study to assess the link between central sleep apnea and cognitive function
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 200 (actual)
- First submitted
- 27 Feb 2024
- Start date
- 21 Aug 2023
- Primary completion date
- 20 Jan 2025
- Lead sponsor
- Zoll Medical Corporation
- Diseases
- Heart failure
- NCT number
- NCT06313840
What you commit to
- Study type: Observational
- Participants enrolled: 200
- From 21 Aug 2023 to the primary completion date, 20 Jan 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- Prevalence Phase Inclusion Criteria:
- Diagnosed with heart failure with reduced or mildly reduced left ventricular ejection fraction (LVEF \<50%) at least 3 months prior to enrollment
- New York Heart Association (NYHA) functional class II-IV
- Treated and optimized on heart failure guideline directed medical therapy as indicated for at least 4 weeks, including angiotensin receptor-neprilysin inhibitors (ARNI) (or angiotensin converting enzyme inhibitors (ACEI) or angiotensin receptor blocker (ARB)), aldosterone receptor antagonists, beta-blockers and/or sodium glucose co-transporter 2 (SGLT-2) antagonists
- Age 50 years or older
- Signed Institutional Review Board (IRB) or Ethics Committee (EC) approved informed consent
- In the opinion of the investigator, subject is willing and able to comply with the protocol, including the cognitive function assessment
- Prevalence Phase Exclusion Criteria:
- Hospitalized for heart failure-related complications in the last 4 weeks
- History of SDB and/or prior or ongoing treatment for SDB or tested for SDB within the prior year
- Cognitive Phase Inclusion Criteria:
- AHI ≥ 15 events per hour and CAHI ≥ 50% of total AHI (Case group) or AHI \< 5 events per hour (Control group) based on the baseline HSAT
- Per the patient and investigator, willing and able to postpone CSA treatment until completion of the study assessment visit (Visit 3)
- Cognitive Phase Exclusion Criteria:
- Color blindness
- Currently taking opioids
- Has taken medications for memory/cognition within the last 3 months (including but not limited to cholinesterase inhibitors and/or glutamate regulators)
- Cerebrovascular accident (stroke or transient ischemic attack) in the last 12 months
- Diagnosed with neurological disease including but not limited to history of seizures, meningitis, traumatic brain injury, amyotrophic lateral sclerosis, multiple sclerosis, attention-deficit/hyperactivity disorder (ADHD) or autism.
Age in the registry: 50 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Szpital Uniwersytecki we Wrocławiu Coordinator of this site? Confirm its status | Wroclaw | Poland | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.