Covid19 Clinical Trial
— CARTESIANOfficial title:
Covid-19 Effects on ARTErial StIffness and Vascular AgiNg
The purpose of the study is to evaluate the presence of early vascular aging 6 months and 12 months after COVID-19 infection.
Status | Recruiting |
Enrollment | 360 |
Est. completion date | March 2033 |
Est. primary completion date | March 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - age >18 years, both sexes; - written informed consent; - affiliation to a social security regime; - a recent diagnosis of COVID19 (6±3 months) proven by PCR or serology (for group 1,2,3) - hospitalization in intensive care unit for COVID19 (for group 1) - hospitalization in a medicine unit for COVID19 (for group 2) - no hospitalization for COVID19 or hospitalization less than 24h (for group 3) - a negative test for SARS-nCOV2 infection (PCR or serology)(for group 4) Exclusion Criteria: - Age <18 years - Inability to express consent of the study - Diseases carrying out a life -expectancy <1 year according to clinical judgment - Pregnancy and breastfeeding - Foreseen inability to attend scheduled visits |
Country | Name | City | State |
---|---|---|---|
France | CHRU Nancy | Nancy | |
France | Hôpital Européen Georges Pompidou - APHP | Paris | |
France | CHU Rouen | Rouen |
Lead Sponsor | Collaborator |
---|---|
Assistance Publique - Hôpitaux de Paris | Institut National de la Santé Et de la Recherche Médicale, France, The Association for Research into Arterial Structure and Physiology |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | total mortality | individual data will be meta-analyzed with sister studies running in parallel worldwide | 2 years | |
Other | total mortality | individual data will be meta-analyzed with sister studies running in parallel worldwide | 5 years | |
Other | total mortality | individual data will be meta-analyzed with sister studies running in parallel worldwide | 10 years | |
Other | CV events | fatal+non-fatal | 2 years | |
Other | CV events | fatal+non-fatal | 5 years | |
Other | CV events | fatal+non-fatal | 10 years | |
Primary | PWV | carotid-femoral pulse wave velocity measured by application tonometry | 6 months after COVID19 infection | |
Primary | PWV | carotid-femoral pulse wave velocity measured by application tonometry | 12 months after COVID19 infection | |
Primary | PWV change | carotid-femoral pulse wave velocity measured by application tonometry | difference between PWV at 12 and 6 months after COVID19 infection | |
Secondary | arterial distensibility | carotid, radial and digital distensibility by standard and ultrahigh frequency ultrasound | 6 months after COVID19 infection | |
Secondary | arterial distensibility | carotid, radial and digital distensibility by standard and ultrahigh frequency ultrasound | 12 months after COVID19 infection | |
Secondary | arterial distensibility change | carotid, radial and digital distensibility by standard and ultrahigh frequency ultrasound | difference between arterial distensibility at 12 and 6 months after COVID19 infection | |
Secondary | brachial artery FMD | brachial artery flow-mediated dilation for non-invasive evaluation of endothelial dysfunction, by ultrasound and automatic edge detection analysis | 6 months after COVID19 infection | |
Secondary | brachial artery FMD | brachial artery flow-mediated dilation for non-invasive evaluation of endothelial dysfunction, by ultrasound and automatic edge detection analysis | 12 months after COVID19 infection | |
Secondary | brachial artery FMD change | brachial artery flow-mediated dilation for non-invasive evaluation of endothelial dysfunction, by ultrasound and automatic edge detection analysis | difference between FMD at 12 and 6 months after COVID19 infection | |
Secondary | central blood pressure | central blood pressure obtained non-invasively by application tonometry and validated transfer function | 6 months after COVID19 infection | |
Secondary | central blood pressure | central blood pressure obtained non-invasively by application tonometry and validated transfer function | 12 months after COVID19 infection | |
Secondary | central blood pressure (BP) change | central blood pressure obtained non-invasively by application tonometry and validated transfer function | difference between central BP at 12 and 6 months after COVID19 infection | |
Secondary | wave separation/wave intensity analysis (WSA/WIA) | peripheral arterial waveform analysis aimed at exploring wave reflection and micro-macrocirculation crosstalk | 6 months after COVID19 infection | |
Secondary | wave separation/wave intensity analysis (WSA/WIA) | peripheral arterial waveform analysis aimed at exploring wave reflection and micro-macrocirculation crosstalk | 12 months after COVID19 infection | |
Secondary | WSA/WIA change | peripheral arterial waveform analysis aimed at exploring wave reflection and micro-macrocirculation crosstalk | difference between WSA/WIA at 12 and 6 months after COVID19 infection | |
Secondary | cardiac diastolic dysfunction | E/e' at rest and after low-level exercise | 6 months after COVID19 infection | |
Secondary | cardiac diastolic dysfunction | E/e' at rest and after low-level exercise | 12 months after COVID19 infection | |
Secondary | cardiac diastolic dysfunction change | E/e' at rest and after low-level exercise | difference between cardiac diastolic dysfunction at 12 and 6 months after COVID19 infection | |
Secondary | myocardial stiffness | cardioelastography by ultrafast ultrasound | 6 months after COVID19 infection | |
Secondary | myocardial stiffness | cardioelastography by ultrafast ultrasound | 12 months after COVID19 infection | |
Secondary | myocardial stiffness change | cardioelastography by ultrafast ultrasound | difference between myocardial stiffness at 12 and 6 months after COVID19 infection | |
Secondary | carotid femoral and hearth carotid change | Mesure by laser doppler vibrometry | 6 months after COVID19 infection |
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