The Effect of Dietary Intervention on Endothelial Glycocalyx in Psoriasis

May 14, 2023 updated by: Ignatios Ikonomidis, University of Athens

The Effect of Dietary Intervention on Endothelial Glycocalyx Integrity and Microvascular Perfusion in Patients With Psoriatic Disease

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 psoriatic disease.

Study Overview

Detailed Description

Sixty patients with psoriatic disease, who are referred to the outpatient psoriasis clinic of the Attikon University Hospital, will be randomized to receive food supplement Endocalyx (4 capsules per day) (n=30) or placebo (n=30) for 4 consecutive months.

Study Type

Interventional

Enrollment (Anticipated)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: Ignatios Ikonomidis, Professor
  • Phone Number: +302105832187
  • Email: ignoik@gmail.com

Study Contact Backup

Study Locations

    • Attiki
      • Athens, Attiki, Greece, 12462
        • Recruiting
        • Attikon University Hospital
        • Contact:
          • Ignatios Ikonomidis, Professor
          • Phone Number: +302105832187
          • Email: ignoik@gmail.com
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Caucasian patients with psoriatic disease (plaque-type psoriasis or psoriatic arthritis)
  • Body mass index ≥18.5 Kg/m2
  • If female, patients must be non-pregnant and non-breastfeeding

Exclusion Criteria:

  • 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
  • Liver failure
  • Malignancies

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Food supplement Endocalyx
Thirty patients with psoriatic disease will randomized to receive 4 capsules a day of the food supplement Endocalyx for 4 months
Patients with psoriatic disease will be randomized to receive food supplement Endocalyx for 4 months.
Other Names:
  • Endocalyx
  • Q-prime
Placebo Comparator: Placebo
Thirty patients with psoriatic disease will randomized to receive 4 capsules a day of the placebo for 4 months
Patients with psoriatic disease will be randomized to receive placebo for 4 months.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Endocalyx effects on endothelial glycocalyx thickness
Time Frame: four months
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 Outcome Measures

Outcome Measure
Measure Description
Time Frame
Endocalyx effects on arterial stiffness
Time Frame: four months
Endocalyx effects on arterial stiffness as assessed by carotid to femoral pulse wave velocity (PWV, m/s) using tonometry.
four months
Endocalyx effects on coronary microcirculation
Time Frame: four months
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 after bolus intravenous adenosine infusion to coronary flow velocity at rest.
four months
Endocalyx effects on left ventricular myocardial function
Time Frame: four months
Endocalyx effects on left ventricular function as assessed by global longitudinal strain using speckle-tracking echocardiography.
four months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ignatios Ikonomidis, Professor, 2nd Cardiology Department, National and Kapodistrian University of Athens

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2022

Primary Completion (Anticipated)

November 1, 2023

Study Completion (Anticipated)

January 30, 2024

Study Registration Dates

First Submitted

December 20, 2021

First Submitted That Met QC Criteria

January 7, 2022

First Posted (Actual)

January 11, 2022

Study Record Updates

Last Update Posted (Actual)

May 16, 2023

Last Update Submitted That Met QC Criteria

May 14, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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