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Active Not Recruiting NCT06766968

Prolonged Compression Following Foam Sclerotherapy

Conditions: Chronic Venous Disorder, Varicose Veins Leg

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 140
Sponsor: Pirogov Russian National Research Medical University

Location: MedSwiss Private Clinic Moscow Moscow

Summary

Foam-form sclerotherapy is an effective method for eliminating varicose veins, which can be used alone or in combination with other interventions (laser or radiofrequency ablation, cyanoacrylate glue embolization) in the treatment of chronic venous disease of the lower limbs. Sclerotherapy is utilized to address both primary and recurrent varicose veins, and it is associated with a low rate of complications. Among the adverse effects, the most common is skin hyperpigmentation (darkening of the skin with the formation of stripes of shades of brown directly above the treated veins), with an occurrence rate reaching 6-53% within the first month following the procedure. Still, it resolves independently in 70% of cases within 6 months. An essential component of sclerotherapy is compression therapy through bandages or medical stockings, which helps accelerate the absorption of veins and improve the aesthetic results of treatment. Meanwhile, the optimal duration for wearing compression stockings after performing foam-form sclerotherapy of varicose tributaries has not been established.

Eligibility Criteria

Inclusion Criteria: * Age over 18 years; * Varicose veins of the lower extremities of clinical class C2 according to CEAP (Clinical, Etiological, Anatomical, Pathophysiological) classification; * Scheduled foam-form sclerotherapy of varicose tributaries as an independent intervention or after trunkal ablation; * Absence of initial skin pigmentation, including that associated with previously performed trunk ablation; * Absence of indications for long-term use of compression therapy, including the clinical class of chronic venous disease C3-C6 and persistence of vein-specific symptoms; * Signed informed consent to participate in the study. Exclusion Criteria: * History of deep vein thrombosis; * Contraindications or restrictions to foam-form sclerotherapy; * Contraindications or restrictions to long-term use of compression therapy; * Inability or difficulty in independently putting on MCS; * Refusal to participate in the study.

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT06766968). StuddyBuddy aggregates publicly available trial information.