MedTrace Logo

Tolerance Study of the Silicone Bands on Medical Compression Stockings

NCT01486225 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 3

Last updated 2014-08-08

No results posted yet for this study

Summary

The purpose of this study is to identify the nature of skin lesions that develop on contact with the grip-top bands of medical compression stockings, which are composed mainly of silicone.

Conditions

  • Skin Lesions

Interventions

DEVICE

Innothera's brand Stockings

15 patients having used Innothera branded Stocking

OTHER

Stockings other than Innothera's brand

15 patients having used any other brand than Innothera's brand stockings

Sponsors & Collaborators

  • Laboratoires Innothera

    lead INDUSTRY

Principal Investigators

  • Annick BARBAUD, MD Professor · Central Hospital, Nancy, France

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-11-30
Primary Completion
2013-10-31
Completion
2013-10-31

Countries

  • France

Study Locations

More Related Trials

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 NCT01486225 on ClinicalTrials.gov