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Clinical Trial Summary

Endothelial dysfunction is assessed in patients with chronic venous insufficiency of lower limbs (grade C4 according to C - clinical manifestations, E - etiologic factors, A - anatomic distribution of disease, and P - underlying pathophysiologic findings (CEAP) classification) prior to and after endovenous surgical procedure, i.e. endovenous laser ablation of great saphenous vein, microphlebectomy of varicose branches. Two treatment groups (with and without additional pharmacotherapy) are compared.


Clinical Trial Description

Each patient will be examined 4 times: Visit 1 (day -1) - collecting and documenting patients' complaints and medical history - local examination - ultrasound angiography of the lower limbs veins - assessment of clinical grade according to CEAP classification Visit 2 (day 0) - assessment of venous disease severity according to Venous Clinical Severity Score (VCSS) - assessment of quality of life with Chronic Venous Insufficiency Quality of Life Questionnaire (CIVIQ-20) - assessment of clinical grade according to CEAP classification - measurement of microcirculation in the operated limb by laser flowmetry using portable device (laser Doppler flowmetry (LDF) registration will be performed on leg anterior surface (lower third) for 10 minutes) - assesment of blood laboratory parameters of endothelial dysfunction: homocysteine, von Willebrand factor, plasminogen activator inhibitor-1 (PAI-1), E-selectin, P-selectin, soluble intercellular adhesion molecule-1 (sICAM-1), soluble vascular endothelial cell adhesion molecule-1 (sVCAM-1) - flow cytometry analysis of circulating cells expressing surface markers (clusters of differentiation (CD)): CD 45-, CD 34+, CD 146+, CD 31+, CD 105+ and CD 309+ - surgical treatment is performed as endovenous laser ablation of GSV and microphlebectomy of varicose branches according to a standard protocol - patients' randomization (method of random numbers) into 2 treatment groups of 20 subjects each with sulodexide treatment (250 LSU bid for 30 day) for the active treatment group and without any additional pharmacotherapy for the control group Visit 3 (day 4 after intervention) - ultrasound angiography of the operated limb (evaluation of the venous ablation and examination of endothermal heat-induced thrombosis (EHIT)) Visit 4 (day 32 after intervention) - collecting and documenting patients' complaints - local examination - ultrasound angiography of the lower limbs veins - assessment of clinical grade according to CEAP classification - assessment of venous disease severity according to VCSS - assessment of quality of life with CIVIQ-20 - measurement of microcirculation in the operated limb by laser flowmetry using portable device - assesment of blood laboratory parameters of endothelial dysfunction: homocysteine, von Willebrand factor, PAI-1, E-selectin, P-selectin, sICAM-1, sVCAM-1 - flow cytometry analysis of circulating cells expressing surface markers: CD 45-, CD 34+, CD 146+, CD 31+, CD 105+ and CD 309+ ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04180137
Study type Interventional
Source State Budgetary Healthcare Institution, National Medical Surgical Center N.A. N.I. Pirogov, Ministry of Health of Russia
Contact
Status Completed
Phase N/A
Start date November 28, 2019
Completion date July 30, 2021

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