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OpenTrials
Completed

NCT Number: NCT06290973

Quality of Life and Health Perception After Surgery of Varicose Veins

The aim of this study is to analyze changes in health perception and quality of life in patients after surgery for varicose veins using clinical score VCSS and QoL scores SF12 as general health questionary and Veines QoL/Sym as disease specific questionary.

Completed

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Hospital CLínico Universitario de Valladolid

Valladolid, Spain

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients with reflux in saphenous vein

Exclusion criteria

  • no reflux in saphenous vein

Treatment and study plan

surgery of varicose veins

Procedure

including ablation with radiofrequency, phlebectomy and saphenectomy.

Primary outcomes

  1. changes in qol questionarie SF-12 after surgery of varicose veins

    Time frame: before and 90 days after surgery

    measured in SF-12 score

  2. changes in qol questionarie Veines QoL/Sym after surgery of

    Time frame: before and 90 days after surgery

    measured in Veines Qol/Sym score

Secondary outcomes

  1. changes in VCSS after surgery of varicose veins

    Time frame: before and 90 days after surgery

    measured in VCSS score

Sponsors and collaborators

Lead sponsor

Hospital Clínico Universitario de Valladolid

Other

Registry information

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Mar 4, 2024
Registry last updated
Mar 4, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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