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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04558450
Other study ID # APHP200762
Secondary ID APHP20076220.07.
Status Recruiting
Phase N/A
First received
Last updated
Start date September 21, 2020
Est. completion date March 2033

Study information

Verified date November 2021
Source Assistance Publique - Hôpitaux de Paris
Contact Rosa Maria BRUNO, MD
Phone +33 1 53 98 79 67
Email rosa-maria.bruno@inserm.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to evaluate the presence of early vascular aging 6 months and 12 months after COVID-19 infection.


Description:

After being informed about the study and potential risks, all eligible patients giving written informed consent will undergo a comprehensive non-invasive assessment of vascular and cardiac function 6 months and 12 months after COVID-19 infection. Cardiovascular events and mortality will be collected 2, 5 and 10 years after inclusion


Recruitment information / eligibility

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

Study Design


Intervention

Diagnostic Test:
carotid-femoral pulse-wave velocity
early vascular aging tests

Locations

Country Name City State
France CHRU Nancy Nancy
France Hôpital Européen Georges Pompidou - APHP Paris
France CHU Rouen Rouen

Sponsors (3)

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

Country where clinical trial is conducted

France, 

Outcome

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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