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UnknownNCT03041337

Right Heart International NETwork During Exercise in Different Clinical Conditions

Morphological and Functional Response of the Right Heart and Pulmonary Circulation

Status
Unknown
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Azienda Ospedaliera OO.RR. S. Giovanni di Dio e Ruggi D'Aragona · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Accepted

Summary

The aim of this registry will be to compare the pathophysiological response of the morphology and function of the right heart and pulmonary circulation assessed with resting and stress-echocardiography in patients with various cardiovascular diseases, to compare them to healthy individuals. The physiological response in healthy individuals as well as elite athletes, defined as athletes participating at national and international competitions, will also be evaluated. Patients will be enrolled both prospectively as well as retrospectively and the will be evaluated by resting and stress echocardiography, which are part of the routine clinical practice. All clinical outcome measures will be collected as part of routine examinations. The measurements will include systolic and diastolic pump function of the right and left ventricles and other echocardiographic parameters. Moreover, a comparison of these parameters among different groups will be performed. Other optional assessments will include: exercise capacity assessed with 6-minute walking distance, World Health Organization functional class (WHO functional class), peak oxygen uptake assessed by spiroergometry. Patients will be evaluated at baseline and each year with the aforementioned procedures according to the sites clinical routine.

Detailed description

Patients will be evaluated with a routinely performed resting and stress echocardiography. Moreover, physical examination and ECG will be performed and past medical history will be collected. Optional procedures comprise of quality of life assessment (SF-36 questionnaire), six minute walking distance (6MWD), cardiopulmonary exercise testing (CPET), routine laboratory including biochemical work-up. Comparison among different cohorts of patients with regards to right heart morphology and function at rest, assessed during a routinely performed resting and stress echography. The following parameters will be evaluated: * Right ventricular (RV) diameters * RV free wall thickness * End-diastolic and end-systolic left ventricular volumes and ejection fraction * Right atrial (RA) area * End-diastolic and end-systolic RV area and % shortening of the areas of the right ventricle * Tricuspid regurgitation velocity (TRV) and severity * Tricuspid annular plane systolic excursion (TAPSE) * Inferior vena cava diameter and % of collapsibility * TAPSE at peak exercise and after 5 minutes recovery * TRV at peak exercise and after 5 minutes recovery * RV end-diastolic and end-systolic area and % shortening of the areas at peak exercise and after 5 minutes recovery * RA area at peak exercise and after 5 minutes recovery * Left ventricular end-diastolic and end-systolic volume and ejection fraction at peak exercise and after 5 minutes recovery * Left ventricular eccentricity index at peak exercise and after 5 minutes recovery

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTstress echocardiographystress echocardiography will be performed in accordance with the current guidelines on a variable load 45° cycle ergometer with an incremental workload of 25 W every 2 minutes up to the symptom-limited maximal tolerated workload. Echocardiographic measurements will be acquired at baseline, at peak exercise and during recovery of 5 minutes. The electrocardiogram and blood pressure will be monitored at each workload. Termination criteria and / or positive test criteria for inducible myocardial ischemia will follow the current recommendations

Timeline

Start date
2015-06-01
Primary completion
2020-01-01
Completion
2025-01-01
First posted
2017-02-02
Last updated
2017-02-02

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT03041337. Inclusion in this directory is not an endorsement.