CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 40 enrolled
Drug / intervention
geko devicedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02137499
NCT02137499N/ACompleted
CompareCT.gov

Venous Insufficiency and Neuromuscular Stimulation

Imperial College London·interventional·Posted May 13, 2014·Updated Oct 25, 2019

In Brief

A clinical study evaluating geko device for Chronic Venous Disease and 2 related conditions. Completed, enrolled 40 participants across 1 site.

Detailed Summary

The investigators will be evaluating the immediate and longer term effect of treatment with a medical device on the symptoms of chronic venous disease.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsChronic Venous Disease, Venous Insufficiency, Deep Venous Obstruction
CountriesUnited Kingdom
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedMay 13, 2014
Enrollment StartAug 1, 2013
Primary CompletionJul 1, 2014
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 12.1 years ago

Interventions

geko devicedevice

Small transcutaneous electrical stimulator. Manufactured in UK by Firstkind UK Ltd, and licensed for use in humans