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Chemoreflex Sensitivity in HFpEF

Chemoreflex Sensitivity in Heart Failure With Preserved Ejection Fraction

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06309537
Acronym
CHEMO-HFpEF
Enrollment
60
Registered
2024-03-13
Start date
2024-10-31
Completion date
2029-12-31
Last updated
2024-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure With Preserved Ejection Fraction

Brief 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.

Interventions

DIAGNOSTIC_TESTchemoreflex evaluation

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

Sponsors

Istituto Auxologico Italiano
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
difference in chemoreflex sensitivity between HFpEF and healthy controls5 years

Countries

Italy

Contacts

Primary ContactSergio Caravita, MD, PhD
s.caravita@auxologico.it+39 02 619112930

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026