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Surgical Revascularisation and Nerve Stimulation Trial

NCT01938924 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2019-07-15

No results posted yet for this study

Summary

A study to investigate if the gekoTM device improves flow through vascular bypass grafts

Conditions

  • Peripheral Arterial Occlusive Disease

Interventions

DEVICE

GekoTM

electrical neuromuscular stimulation

Sponsors & Collaborators

  • Hull University Teaching Hospitals NHS Trust

    lead OTHER_GOV

Principal Investigators

  • Rachel Barnes, MRCS, MA · Hull Royal Infirmary

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2014-12-31
Completion
2014-12-31

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 NCT01938924 on ClinicalTrials.gov