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DESIVI: Dosing of Electrical Stimulation in Venous Insufficiency

NCT03850496 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2020-07-31

Study results available
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Summary

This study is designed to describe the difference in varicose vein outcomes found from using a neuromuscular electrical stimulation device for different amounts of time - Group A (control - no device), Group B (device for 30 mins per day) and Group C (device for 60 mins per day). The groups are assessed after 6 weeks of intervention.

Conditions

  • Varicose Veins
  • Venous Stasis
  • Venous Insufficiency

Interventions

DEVICE

Revitive IX Neuromuscular Stimulation Device

Neuromuscular stimulation footplate device with a pre-programmed 30 minute varying electrical stimulation sequence.

Sponsors & Collaborators

  • Actegy Ltd.

    collaborator INDUSTRY

  • Imperial College London

    lead OTHER

Principal Investigators

  • Raveena Ravikumar, MRCS · Imperial College London

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-11-01
Primary Completion
2016-08-31
Completion
2016-10-31

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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 NCT03850496 on ClinicalTrials.gov