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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05185934
Other study ID # 668/30-11-2021
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 1, 2022
Est. completion date January 30, 2024

Study information

Verified date May 2023
Source University of Athens
Contact Ignatios Ikonomidis, Professor
Phone +302105832187
Email ignoik@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The food supplement Endocalyx is considered to support the endothelial glycocalyx integrity by supplying sulfated polysaccharides, anti-oxidant enzymes and additional substrates for glycocalyx synthesis. The investigators will study the effect of Endocalyx on endothelial, vascular and left ventricular myocardial function in patients with COVID-19 infection.


Description:

Sixty patients who have been hospitalized due to COVID-19 infection will be randomized to receive food supplement Endocalyx (4 capsules per day) (n=30) or placebo (n=30) for 4 consecutive months.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date January 30, 2024
Est. primary completion date November 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - caucasian patients - hospitalization for COVID-19 infection - diagnosis of COVID-19 proven by PCR Exclusion Criteria: - Pregnancy and breastfeeding - Foreseen inability to attend scheduled visits - History of acute coronary syndrome. Coronary artery disease will be excluded by a clinical history, examination and electrocardiogram. - Moderate or severe valve disease - Primary cardiomyopathies - Chronic obstructive pulmonary disease - Asthma - Chronic kidney disease (estimated glomerular filtration rate [eGFR] =60 ml/min/1.73 m2) - Liver failure - Malignancies

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Food supplement Endocalyx
Patients with COVID-19 infection will be randomized to receive food supplement Endocalyx for 4 months.
Placebo
Patients with COVID-19 infection will be randomized to receive placebo for 4 months.

Locations

Country Name City State
Greece "Attikon" University General Hospital Athens Attiki

Sponsors (1)

Lead Sponsor Collaborator
University of Athens

Country where clinical trial is conducted

Greece, 

Outcome

Type Measure Description Time frame Safety issue
Primary Endocalyx effects on endothelial glycocalyx thickness Endocalyx effects on endothelial glycocalyx thickness as assessed by perfused boundary region (PBR, micrometers) of the sublingual arterial microvessels using Sidestream Dark Field (SDF) imaging four months
Secondary Endocalyx effects on arterial stiffness Endocalyx effects on arterial stiffness as assessed by carotid to femoral pulse wave velocity (PWV, m/s) using tonometry. four months
Secondary Endocalyx effects on coronary microcirculation Endocalyx effects on coronary function as assessed by measuring coronary flow reserve of left anterior descending artery. Coronary flow reserve is estimated by Doppler echocardiography as the ratio of coronary flow velocity (m/s) after bolus intravenous adenosine infusion to coronary flow velocity (m/s) at rest. four months
Secondary Endocalyx effects on left ventricular myocardial function Endocalyx effects on left ventricular function as assessed by global longitudinal strain using speckle-tracking echocardiography. four months
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