Ireland
--:--IST
Starting soon Observational

Chemoreflex Sensitivity in HFpEF

NCT06309537 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2024-10
Last updated
2024-03-13

Condition(s) studied

Heart Failure With Preserved Ejection Fraction

Investigational drug(s) / intervention(s)

chemoreflex evaluation

chemoreflex evaluation: the ventilatory response to carbon dioxide and hypoxia will be assessed in study participants

Study summary

Patients with heart failure and a preserved left ventricular ejection fraction (HFpEF) almost invariably complain of exertional breathlessness. Abnormal cardiac hemodynamics with pulmonary congestion are believed to trigger dyspnea in this patients. However, some patients may complain of exertional breathlessness which seems to be out of proportion as compared with hemodynamic abnormalities.

Chemoreflex sensitivity accounts for the ventilatory responses to a variety of chemical stimuli, including carbon dioxide produced by the organism during exercise. Chemoreflex sensitivity can be augmented in heart failure with reduced left ventricular ejection fraction, and an increased chemoreflex sensitivity has been linked to symptoms, neurohumoral activation, breathing disturbances, and adverse prognosis.

However, the clinical correlates and implications of chemoreflex sensitivity in HFpEF have not been accurately studied.

We aim to characterize chemoreflex sensitivity in patients with a diagnosis of HFpEF, and to correlate chemoreflex sensitivity with clinical and hemodynamic characteristics.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * diagnosis of symptomatic HFpEF (group 1) * diagnosis of asymptomatic left ventricular diastolic dysfunction with echocardiographic signs of PH (group 2) * healthy volunteers (group 3) Exclusion Criteria: * breastfeeding or childbearing

Primary outcome measure(s)

  • difference in chemoreflex sensitivity between HFpEF and healthy controls — 5 years

Trial sites (1)

FacilityCityRegionStatus
Ospedale San Luca IRCCS Istituto Auxologico Italiano Milan Italy
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06309537 on ClinicalTrials.gov ↗ ← All trials in Italy