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Ongoing Registry of Treatment of Chronic Venous Diseases

Russian Registry of Treatment of Chronic Venous Diseases

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03035747
Acronym
RRT CVD
Enrollment
5000
Registered
2017-01-30
Start date
2016-07-31
Completion date
2036-07-31
Last updated
2024-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Varicose Veins of Lower Limb

Keywords

registry, varicose veins, conventional surgery, thermal ablation, radiofrequency, laser, sclerotherapy

Brief summary

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

Detailed description

Data of patients treated in different Russian medical centers are entered in a prospective digital database, and continuously updated. There is planned to conduct prospective randomized, cohort and observational studies on the site of register

Interventions

PROCEDUREconventional surgery

high ligation and stripping of incompetent saphenous veins

endovenous laser ablation of incompetent saphenous veins

PROCEDUREsclerotherapy

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

endovenous radiofrequency ablation of incompetent saphenous veins

PROCEDUREphlebectomy

hooks phlebectomy of varicose veins

Sponsors

Pirogov Russian National Research Medical University
CollaboratorOTHER
Medalp Private Surgery Clinic
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* no

Design outcomes

Primary

MeasureTime frame
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 methodsBaseline, 3 - 6, 12 months post-intervention

Secondary

MeasureTime frameDescription
Change in Quality of Life (QoL), assessed by Short form (SF)-36 health survey (optional)Baseline, 3 and 12 months post-interventionThe SF-36 is a generic QoL questionnaire.
Change in Venous Clinical Severity Score (VCSS) (optional)Baseline, 3 and 12 months post-interventionThe VCSS is a validated scoring system for assessing signs, symptoms and complaints of venous disease.
Change in Quality of Life (QoL), assessed by Aberdeen Varicose Vein Questionnaire (AVVQ) (optional)Baseline, 3 and 12 months post-interventionThe AVVQ is a disease-specific QoL questionnaire aimed at venous disease.

Countries

Russia

Contacts

Primary ContactEvgeny Ilyukhin, MD, PhD
evgeny@ilyukhin.info+79218451722

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026