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UnknownNCT05246423

Ergospirometry in Paroxysmal Atrial Fibrillation Prognosis

Paroxysmal Atrial Fibrillation Prognosis Based on Cardiopulmonary Exercise Test Data and Novel Echocardiographic and Plasma Biochemical Indices (the PLACEBO Trial)

Status
Unknown
Phase
Study type
Observational
Enrollment
80 (estimated)
Sponsor
Aristotle University Of Thessaloniki · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

An observational, prospective, cohort study aiming to assess the potential predictive role of cardiopulmonary exercise testing in the prognosis of paroxysmal atrial fibrillation, in combination with echocardiographic indices and plasma biomarker values.

Detailed description

The "ParoxysmaL Atrial fibrillation prognosis based on Cardiopulmonary Exercise test data and novel echocardiographic and plasma BiOchemical indices" (PLACEBO) trial comprises an observational, prospective, single-center cohort study including patients with paroxysmal atrial fibrillation. All patients undergo clinical examination, detailed echocardiographic study, cardiopulmonary exercise testing (CPET) and 24-hour ambulatory echocardiographic monitoring (24-hour Holter monitoring), as well as measurement of a series of plasma biochemical indices. The study will examine the potential prognostic role of CPET variables (such as peak VO2) in the future recurrences of paroxysmal atrial fibrillation.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTObservation groupPatients with paroxysmal atrial fibrillation undergo cardiopulmonary exercise testing, echocardiography, 24-hour ambulatory electrocardiographic monitoring and plasma biomarkers' measurement

Timeline

Start date
2020-12-10
Primary completion
2024-12-10
Completion
2024-12-10
First posted
2022-02-18
Last updated
2022-02-18

Locations

1 site across 1 country: Greece

Source: ClinicalTrials.gov record NCT05246423. Inclusion in this directory is not an endorsement.