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Study to Assess the Efficacy and Safety of Endolex Forte VErsus Diosmin and Hesperidin in Reducing VeNous Insufficiency — EVELINE  

Chronic Venous Insufficiency Clinical Trial

Official title:
A Comparative Study to Assess the Efficacy and Safety of Endolex Forte vs Diosmin and Hesperidin in Reducing the symptomatoLogy of Patients With ChronIc VeNous Insufficiency Between Functional Classes CEAP 1-4, During a Period of 6 Months

Clinical Trial Summary

The trial is designed as a randomized, multicenter, open label, comparative, 6 months, clinical study.

Clinical Trial Description

A randomized, multicentered, open label, comparative study to assess the efficacy and safety of Endolex Forte® versus a combination of micronized diosmin (450 mg) and micronized hesperidin (50 mg) in reducing the symptomatology of patients diagnosed with Chronic Venous Insufficiency which is rated between functional classes CEAP 1-4, during a period of 6 months. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02927483
Study type Interventional
Source SunWave Pharma
Contact Dionisio Barattini, MD
Phone +39 335 5437574
Email barattini@operacro.com
Status Not yet recruiting
Phase Phase 3
Start date November 2016
Completion date June 2017
View Details
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