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Isolated Great Saphenous Vein Stripping for Treatment of Varicose Veins in Lower Limbs

NCT07616115 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2026-05-29

No results posted yet for this study

Summary

The goal of this clinical trial is to compare two surgical approaches for treating varicose veins in the lower limbs in adults: performing varicose vein removal at the same time as great saphenous vein stripping (concomitant) versus performing great saphenous vein treatment alone.

The main questions it aims to answer are:

* Do clinical outcomes differ between these approaches?
* Does quality of life improve differently depending on which surgical approach is used?

Participants will:

* Undergo great saphenous vein stripping for lower limb varicose veins with or without simultaneous varicose vein ressection
* Be assigned to have varicose vein resection either at the same time or in a subsequent procedure
* Complete quality of life assessments before and after surgery

Conditions

  • Varicose Veins of Lower Limb
  • Saphenous Vein
  • Venous Insufficiency

Interventions

PROCEDURE

Great saphenous vein stripping

Stripping of the great saphenous vein for the treatment of patients with chronic venous disease of the lower limbs associated with great saphenous vein insufficiency

PROCEDURE

Varicose veins removal

Resection of visible varicose tributaries through staggered mini-incisions

Sponsors & Collaborators

  • Hospital Israelita Albert Einstein

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-01
Primary Completion
2024-02-28
Completion
2024-06-30

Countries

  • Brazil

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07616115 on ClinicalTrials.gov