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RecruitingNCT07451873GlikoOxENDUpdated Mar 9, 2026

Glycocalyx and Oxidative Stress in Endothelial Function (Part 2)

An observational study in Coronary Heart Disease, sponsored by Josip Juraj Strossmayer University of Osijek. Recruiting at 1 site in Croatia. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-03-09.

Sponsored by Josip Juraj Strossmayer University of Osijek · Observational

From the registry’s dates

  • Started Oct 2025; still recruiting 1 year later.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
35
Ages
18 Years and older
Sex
All
01

Study summary

The primary research objective of the project is to determine the role of eGC in microvascular reactivity in patients with coronary heart disease (CHD) before and after bypass grafting (cross-sectional study 2).The main objective of the project is to increase the excellence and interdisciplinarity of scientific work at MEFOS by connecting researchers from different scientific fields, improving conditions and resources for scientific work, and increasing international cooperation, in line with strategic objective 1: raising scientific excellence. The results of the project could provide pathophysiological insight into the development and maintenance of endothelial dysfunction in CVD, as well as identify new biomarkers for CVD.

Read the detailed description

The primary objective of this project is to determine the association between endothelial glycocalyx (eGC) and myocardial revascularization in patients undergoing coronary artery bypass grafting and clinical outcomes of treatment (observational prospective study 2).

Specific objective 2.1: Measure eGC thickness in coronary artery disease patients before and after surgery.

Specific objective 2.2: Determine the reactivity of the bypass graft sample in in vitro experiments.

Specific objective 2.3: Quantify soluble markers of eGC, oxidative stress, and inflammation from serum and PBMC samples, as well as antioxidant capacity.

Specific objective 2.4: Determine the association between the results of functional tests, eGC, and markers from specific objective 2.3 with clinical outcomes of treatment.

02

Conditions studied

  • Coronary Heart Disease

Keywords

  • Glycocalyx
  • Inflammation
  • Oxidative stress
  • Endothelium
  • Coronary Artery Disease
  • Myocardial Revascularization
03

In context

Coronary Disease

2,839 studies on the registry are indexed under Coronary Disease; 311 are open to participants now.

This study's planned enrollment of 35 is below the median of 460 across 953 observational studies indexed under Coronary Disease.

Browse Coronary Disease studies →

Lead sponsor

Josip Juraj Strossmayer University of Osijek is the lead sponsor of 26 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Adult patients undergoing elective coronary artery bypass grafting (CABG)

Inclusion criteria

  • adult patients of both sexes over 18 years of age
  • Caucasian
  • undergoing elective coronary artery bypass grafting (CABG)
  • provided written informed consent

Exclusion criteria

Exclusion Criteria:

  • emergency surgery
  • sepsis or severe systemic inflammation before surgery
  • severe renal or hepatic insufficiency
  • immunosuppression
  • serious comorbidities (e.g., active cancer)
  • therapies that could affect oxidative stress (e.g., high doses of corticosteroids)
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
35 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Coronary Heart Disease (CHD) patients

    Adult patients of both sexes over 18 years of age, undergoing elective coronary artery bypass grafting (CABG) and who provided written informed consent

06

What researchers measure

Primary outcomes

  1. Endothelial glycocalyx

    Measurement of the thickness of endothelial glycocalyx in coronary heart disease patients before and after bypass surgery - measured by Glycocheck

    Time frame: Perioperative/Periprocedural

Secondary outcomes

  1. Bypass graft sample reactivity

    Determine the reactivity of the bypass graft sample in in vitro experiments - measured by isolated vessel setup

    Time frame: Baseline, at one time point

  2. Endothelial glycocalyx soluble markers

    Quantification of soluble markers of endothelial glycocalyx from serum or plasma samples in the specified groups - measured by ELISA assays (syndecan-1, syndecan-4, glypican-1, MMP-9)

    Time frame: Perioperative/Periprocedural

  3. Intracellular oxidative stress production

    Quantification of intracellular oxidative stress production from peripheral blood mononuclear cells (PBMC) in the specified groups - measured by flow cytometry (DCF-DA and DHE)

    Time frame: Perioperative/Periprocedural

  4. Inflammation

    Quantification of inflammation from peripheral blood mononuclear cells (PBMC) in the specified groups - measured by Luminex assay (cytokine profile) and flow cytometry (macrophage frequency)

    Time frame: Perioperative/Periprocedural

  5. Antioxidant capacity

    Quantification of antioxidative enzyme concentration and activation from serum samples in the specified groups - measured by ELISA assays and UV-Vis spectrophotometry (SOD, GPx, CAT)

    Time frame: Perioperative/Periprocedural

  6. Oxidative stress biomarkers

    Quantification of oxidative stress biomarkers from serum samples in the specified groups - measured by ELISA assays (MPO, 8-iso prostaglandin F2a, OxLDL, AOPP)

    Time frame: Perioperative/Periprocedural

Other outcomes

  1. Blood pressure

    Automatic oscillometric measurement of systolic and diastolic blood measurement (mmHg)

    Time frame: Perioperative/Periprocedural

  2. Heart rate

    Automatic oscillometric measurement of heart rate (bpm)

    Time frame: Perioperative/Periprocedural

  3. Body Mass Index

    Measurement of BMI (kg/m2)

    Time frame: Perioperative/Periprocedural

  4. Body composition

    Body composition and body fluid status measurement by a four-terminal portable impedance analyzer. Based on the value of skin resistance (Ohm) empirically derived formulas (the original manufacturer's software) will be used to calculate the estimated Fat Free Mass (FFM kg) and Fat (Fat Mass kg).

    Time frame: Perioperative/Periprocedural

  5. Body fluid status

    Body fluid status measurement by a four-terminal portable impedance analyzer. Based on the value of skin resistance (Ohm) empirically derived formulas (the original manufacturer's software) will be used to calculate the estimated Total Body Water (TBW L), Extracellular Water (ECW L), Intracellular Water (ICW L), Plasma Fluid (PF L) and Interstitial Fluid (IF L).

    Time frame: Perioperative/Periprocedural

07

Study locations

1 of 1 sites recruiting
  • Osijek University Hospital
    Osijek, 31000, Croatia
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07451873
Lead sponsor
Josip Juraj Strossmayer University of Osijek
Responsible party
Ines Drenjancevic (Head of Department of Physiology and Immunology Faculty of Medicine Osijek, Josip Juraj Strossmayer University of Osijek) — Principal investigator
First posted
Mar 5, 2026
Start date
Oct 1, 2025
Primary completion
Sep 30, 2029 (estimated)
Completion
Sep 30, 2029 (estimated)
Last update
Mar 9, 2026

Study contacts

Ines Drenjančević, MD, PhD
Contact
ines.drenjancevic@mefos.hr
+385912241406

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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