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GEKO Venous Thromboembolism Prevention Study
Sponsor: Firstkind Ltd
Summary
This multicentre, randomised geko™ venous thromboembolism (VTE) prevention study will prospectively collect clinical data on VTE occurrences in immobile patients after stroke, who will be randomised, on a 1:1 allocation, to receive either standard of care (Intermittent Pneumatic Compression) or geko™ neuromuscular electrostimulation device. The aim is to assess the prevention of VTE during a follow-up period of 90 days (three months) post-randomisation.
Official title: A Randomised Controlled Trial of the Effectiveness of Intermittent Surface Neuromuscular Stimulation Using the Geko™ Device Compared With Intermittent Pneumatic Compression to Prevent Venous Thromboembolism in Immobile Acute Stroke Patients
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
1200
Start Date
2023-07-06
Completion Date
2025-06-30
Last Updated
2025-03-04
Healthy Volunteers
No
Interventions
geko™ device
Neuromuscular electrical stimulation of the peroneal nerve
Locations (18)
West Suffolk Hospital
Bury St Edmunds, Suffolk, United Kingdom
Royal United Hospital
Bath, United Kingdom
Queen Elizabeth Hospital Birmingham
Birmingham, United Kingdom
The Royal Bournemouth Hospital
Bournemouth, United Kingdom
Fairfield General Hospital
Bury, United Kingdom
Addenbrooke's Hospital
Cambridge, United Kingdom
Kent and Canterbury Hospital
Canterbury, United Kingdom
Countess of Chester Hospital
Chester, United Kingdom
Whiston Hospital
Liverpool, United Kingdom
Northwick Park Hospital
London, United Kingdom
King's College Hospital
London, United Kingdom
Milton Keynes University Hospital
Milton Keynes, United Kingdom
Queen's Medical Centre
Nottingham, United Kingdom
Salford Royal Hospital
Salford, United Kingdom
Stepping Hill Hospital
Stockport, United Kingdom
Royal Stoke University Hospital
Stoke-on-Trent, United Kingdom
New Cross Hospital
Wolverhampton, United Kingdom
Yeovil Hospital
Yeovil, United Kingdom