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Ongoing Registry of Treatment of Chronic Venous Diseases

ConditionVaricose Veins of Lower Limb
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMedalp Private Surgery Clinic

About this trial

Ongoing registration of patients with varicose veins disease treated by means of conventional surgery, endovenous thermal ablations, sclerotherapy, non-tumescent non-thermal methods

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Varicose veins with any source of pathological reflux, C2 - C6 according to the CEAP classification

Disqualifiers

no exclusion criteria

Trial population

Patients undergoing interventions in cases varicose vein disease

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • conventional surgery

    Procedure/Surgery

    high ligation and stripping of incompetent saphenous veins

  • endovenous laser ablation

    Procedure/Surgery

    endovenous laser ablation of incompetent saphenous veins

  • sclerotherapy

    Procedure/Surgery

    ultrasound guided or catheter or or any other methods sclerotherapy of incompetent saphenous or varicose veins

  • endovenous radiofrequency ablation

    Procedure/Surgery

    endovenous radiofrequency ablation of incompetent saphenous veins

  • phlebectomy

    Procedure/Surgery

    hooks phlebectomy of varicose veins

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Change in patency target veins assessed by duplex ultrasonography in different follow up periods after conventional surgery, endovenous thermal ablations, sclerotherapy or non-tumescent non-thermal methods

Time frame
Baseline, 3 - 6, 12 months post-intervention

Secondary outcomes

1

Change in Quality of Life (QoL), assessed by Short form (SF)-36 health survey (optional)

The SF-36 is a generic QoL questionnaire.

Time frame
Baseline, 3 and 12 months post-intervention
2

Change in Venous Clinical Severity Score (VCSS) (optional)

The VCSS is a validated scoring system for assessing signs, symptoms and complaints of venous disease.

Time frame
Baseline, 3 and 12 months post-intervention
3

Change in Quality of Life (QoL), assessed by Aberdeen Varicose Vein Questionnaire (AVVQ) (optional)

The AVVQ is a disease-specific QoL questionnaire aimed at venous disease.

Time frame
Baseline, 3 and 12 months post-intervention

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Medalp Private Surgery Clinic

Lead sponsor

Pirogov Russian National Research Medical University

Collaborator

Source ClinicalTrials.gov
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