Study to Evaluate Impact SANKOM Patent Socks in Patients With CVI

NCT03445091 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2018-03-02

No results posted yet for this study

Summary

Clinical study to evaluate impact on quality of life in patients with Chronic Venous Insufficiency during 4 weeks period of using SANKOM® Patent Socks

Conditions

  • Chronic Venous Insufficiency

Interventions

DEVICE

SANKOM Patent Socks

Using compression socks to ease symptoms of patients with chronic venous insufficiency

Sponsors & Collaborators

  • InterMedService SA

    collaborator OTHER
  • Pharmaxi LLC

    collaborator INDUSTRY
  • Sankom SA

    lead INDUSTRY

Principal Investigators

  • Serge M Mazourik, MD · Intermedservice

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
35 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-05
Primary Completion
2018-04-01
Completion
2018-04-01

Countries

  • Ukraine

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03445091 on ClinicalTrials.gov