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Clinical Trials/NCT05766579
NCT05766579
Recruiting
Not Applicable

ElaStic-compressive Stockings at 21 mmHg and 32 mmHg Following Thermal Ablation of the Great Saphenous Vein.

IRCCS Policlinico S. Donato1 site in 1 country64 target enrollmentApril 2, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Vascular Surgical Procedures
Sponsor
IRCCS Policlinico S. Donato
Enrollment
64
Locations
1
Primary Endpoint
Postoperative Pain
Status
Recruiting
Last Updated
12 months ago

Overview

Brief Summary

Endovascular thermal ablation is currently considered as the best procedure for treating varicose veins thanks to its mini-invasiveness and the lowest rate of incidence of complications. At the end of the endovascular ablation procedure, the European Society of Vascular Surgery (ESVS) guidelines recommend the use of the compression stockings to reduce postoperative pain and the incidence of edema and thrombotic complications.

Despite this, the duration, type and degree of compression to be used, particularly after radiofrequency ablation procedures, remain a matter of debate. Furthermore, although the benefits of postoperative elastic compression therapy are well known, there is various evidence demonstrating how patients often experience poor comfort in wearing stockings, especially those with a higher degree of compression, which causes poor compliance with therapy. In light of all this, each center recommends the use of elastic compression stockings in the postoperative period with a degree of compression that varies, however, according to internal protocols.

There is currently no work in the literature that compares the advantages and disadvantages of using elastic compression stockings with a K2 versus K1 compression degree after radiofrequency ablative surgery.

Registry
clinicaltrials.gov
Start Date
April 2, 2019
End Date
December 31, 2026
Last Updated
12 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
IRCCS Policlinico S. Donato
Responsible Party
Principal Investigator
Principal Investigator

Daniela Mazzaccaro

Medical Doctor and Researcher

IRCCS Policlinico S. Donato

Eligibility Criteria

Inclusion Criteria

  • adult patients (\>18 years) suffering from varicose vein pathology of the lower limbs C2-3 class (varicose veins, edema) according to Clinic, Etiology, Anatomy, Pathophysiology (CEAP) classification, supported by incontinence of the great saphenous vein documented by Echo-Duplex study and candidates for thermal ablation by radiofrequency of the great vein saphenous vein with associated phlebectomy of the ipsilateral thigh and/or leg varices.

Exclusion Criteria

  • Patients who are minors (\< 18 years old) or adults who have not given their consent to participate in the study.
  • Presence of severe obliterating arterial disease of the lower limbs (ABI \<0.5)
  • Obesity (BMI \>30)
  • Varicose pathology of the lower limbs in C4-C6 class according to Clinic, Etiology, Anatomy, Pathophysiology (CEAP) classification (presence of:
  • lipodermatosclerosis/eczema and/or ulcers in progress and/or previous ulcers in the affected lower limb).
  • Pregnancy.

Outcomes

Primary Outcomes

Postoperative Pain

Time Frame: 7 days after surgery

Evaluation of postoperative pain using the Visual Analogic pain Scale (1-10, being higher the pain the higher the value of the scale)

Secondary Outcomes

  • Analgesic Drugs Use(30 days from intervention)
  • Lower limb edema(30 days from intervention)
  • Postoperative Complications(30 days from intervention)
  • Discomfort(30 days from intervention)
  • Evaluation of Quality of Life(30 days from intervention)

Study Sites (1)

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