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Status unknownNCT04436549PAVEDIUpdated Jun 18, 2020

Pathology, Venous Disease, and Clinical Correlations

An observational study in Varicose Veins, Pathology and Symptoms and Signs, sponsored by University of Catanzaro. Status unknown at 2 sites in Italy. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-06-18.

Sponsored by University of Catanzaro · Observational

The sponsor has not verified this record recently (last verified Jun 2020), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
100
Ages
18 Years and older
Sex
All
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Study summary

Chronic Venous Disease (CVD) has a high prevalence in the general population of the western world. Varicose veins are the main signs of this disease that are characterized by important pathological vessel wall changes. There are also several symptoms that affect the quality of life of affected patients. The aim of this study is to correlate the main histopathological abnormalities with the type and the intensity of the symptoms.

Read the detailed description

Chronic Venous Disease (CVD) of the lower limbs is a widespread chronic condition of the western world. There are several signs and symptoms that affect quality of life of patients with CVD. One of the main signs of this disease are varicose veins that are enlarged, swollen, and twisting superficial veins. Vessel wall of varicose veins shows a significant histopathological phenotype, characterized by a distortion of structural architecture: endothelial damage, disorganization of muscle bundles and alteration of the composition of the extracellular matrix (ECM). Symptoms may be different, according to disease state, progression and local inflammatory processes. To date, there is no study that correlate the type and the intensity of symptoms with histopathological phenotype.

Aim of this study is to correlate histopathological phenotype with clinical manifestations.

A cohort of patients with varicose veins scheduled for open surgical treatment that will undergo to stab avulsion of varicose veins will be recruited. Subsequently, venous tissue from stab avulsion will collected in order to evaluate the following biomarkers: VEGF (Vascular -Endothelial Growth Factor), PGP 9.5 (Protein Gene Product 9.5), Fibronectin and Matrix Metalloproteinase- 9 (MMP-9).

VEGF has a key role as a regulator of angiogenesis; its expression is highly regulated by hypoxia, in this case induced by venous hypertension. In addition to being a marker of neoangiogenesis, it increases vascular permeability in inflammatory disorders. PGP 9.5 is a marker of the innervation of the vessel wall that plays an important role in the regulation of venous tone. Fibronectin and MMP-9 are direct markers of ECM remodeling and impairment and they have also a role in chronic inflammation.

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Conditions studied

  • Varicose Veins
  • Pathology
  • Symptoms and Signs

Keywords

  • pathology
  • varicose veins
  • chronic venous disease
  • symptoms
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In context

Varicose Veins

258 studies on the registry are indexed under Varicose Veins; 36 are open to participants now.

This study's planned enrollment of 100 is below the median of 124 across 81 observational studies indexed under Varicose Veins.

Browse Varicose Veins studies →

Lead sponsor

University of Catanzaro is the lead sponsor of 45 studies on the registry; 2 are open to participants now.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with varicose veins that are scheduled to undergo surgery for varicose veins removal.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients with varicose veins scheduled for surgery

Exclusion criteria

Exclusion Criteria:

  • Peripheral artery disease
  • Malignancy
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Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • Patients with varicose veins

    Patients with varicose veins and eligible to receive open surgery (stab avulsion of varicose veins) as routinely care.

    Procedure: Stab Avulsion of varicose veins · Diagnostic Test: Histopathologic evaluation of varicose veins

Interventions

  • ProcedureStab Avulsion of varicose veins

    Stab avulsion is a technique to remove varicose veins. In this procedure, several tiny cuts (incisions) are made in the skin through which the varicosed vein is removed. Removed varicose veins will be collected and analyzed.

    Also known as: Phlebectomy

  • Diagnostic testHistopathologic evaluation of varicose veins

    Sample obtained from varicose veins of lower limbs of patients will be collected and immediately fixed in formalin. The tissue fragments will be taken from varicose veins. Subsequently the tissue will be embedded in paraffin and 3-to-4 mm thick sections will be prepared by a microtome. The tissue sections will be processed for histological and immunohistochemical studies of VEGF, MM9, PGP 9.5 AND FRIBRONECTIN. For antibodies the EnVision staining system (Dako EnVision™) will be used. For the analysis of the positive structures detected by immunohistochemistry, a semiquantitative evaluation method will be used.

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What researchers measure

Primary outcomes

  1. Expression of Matrix Metalloproteinase-9 (MMP-9)

    EnVision staining system (Dako EnVision™) will be used. A synthetic peptide from the middle region of human MMP9 will be used with dilutions 1:50 with Ethylenediaminetetraacetic acid (EDTA).

    Time frame: at 10 month

  2. Expression of Vascular Endothelial Growth Factor (VEGF)

    EnVision staining system (Dako EnVision™) will be used. Monoclonal mouse Anti-Human vascular endothelial growth factor, code No. M7273 will be used with dilution 1:50 with Ethylenediaminetetraacetic acid (EDTA).

    Time frame: at 10 month

  3. Expression of Fibronectin

    EnVision staining system (Dako EnVision™) will be used. A synthetic peptide made toward the C-terminal region of the human Fibronectin protein (within residues 2250-2300) will be used with dilution 1:400 citrate buffer.

    Time frame: at 10 month

  4. Expression of Protein Gene Product 9.5 (PGP 9.5)

    EnVision staining system (Dako EnVision™) will be used. Purified PGP 9.5 isolated from bovine brain will be used with dilution 1:200 citrate buffer

    Time frame: at 10 month

Secondary outcomes

  1. Correlation of the biomarkers expression with signs and symptoms

    The expression of the biomarkers that will be studied on venous tissue samples will be correlated with the type of signs and symptoms complained by the patients.

    Time frame: At 11 month.

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Study locations

2 of 2 sites recruiting
  • CIFL- Interuniversity Center of Phlebolymphology
    Catanzaro, 88100, Italy
    Recruiting
  • University Magna Graecia of Catanzaro
    Catanzaro, 88100, Italy
    • Raffaele Serra, M.D., Ph.D. · Contact · rserra@unicz.it · +3909613647380
    Recruiting
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References and documents

Publications

  • Birdina J, Pilmane M, Ligers A. The Morphofunctional Changes in the Wall of Varicose Veins. Ann Vasc Surg. 2017 Jul;42:274-284. doi: 10.1016/j.avsg.2016.10.064. Epub 2017 Mar 11. PubMed 28300675 ↗
  • Kucukguven A, Khalil RA. Matrix metalloproteinases as potential targets in the venous dilation associated with varicose veins. Curr Drug Targets. 2013 Mar;14(3):287-324. PubMed 23316963 ↗
  • Kolano P, Bednarski IA, Lesiak A, Skibinska M, Stasikowska-Kanicka O, Danilewicz M, Narbutt J. Overexpression of cathepsin K and vascular endothelial growth factor in chronic venous ulcerations. Postepy Dermatol Alergol. 2020 Apr;37(2):234-239. doi: 10.5114/ada.2020.94840. Epub 2020 May 6. PubMed 32489360 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 18, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04436549
Lead sponsor
University of Catanzaro
Responsible party
Prof. Raffaele Serra, MD, Ph.D. (Associate Professor of Vascular Surgery, University of Catanzaro) — Principal investigator
First posted
Jun 18, 2020
Start date
Dec 1, 2019
Primary completion
Sep 1, 2020 (estimated)
Completion
Oct 1, 2020 (estimated)
Last update
Jun 18, 2020

Study contacts

Raffaele Serra, M.D., Ph.D.
Contact
rserra@unicz.it
+3909613647380
Raffaele Serra, M.D., Ph.D.
principal investigator · University Magna Graecia of Catanzaro

Oversight

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

Not currently enrolling

This study is status unknown, as verified in Jun 2020. You cannot join it, but the record below documents what was studied.

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