Geko Venous Leg Ulcer Study

NCT02482038 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2020-03-24

No results posted yet for this study

Summary

This study is designed to look at the effect of the geko device on the circulation in lower limbs of participants with venous leg ulcers.

Conditions

  • Venous Leg Ulcer

Interventions

DEVICE

geko

neuromuscular electrostimulator

Sponsors & Collaborators

  • Firstkind Ltd

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2018-06-05
Completion
2019-10-10

Countries

  • United Kingdom

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 NCT02482038 on ClinicalTrials.gov