Condition: Stroke, Acute · Venous Thromboembolism · Deep Vein Thrombosis · Sponsor: Firstkind Ltd
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.
This description comes directly from the study's public registry record.
Kieron Day, DPhil · +44 (0) 7921 106253 · Kieron.Day@firstkindmedical.com
Wing To, PhD · +44 (0) 7827 612109 · wing.to@firstkindmedical.com
Always discuss trial participation with your own doctor first.
| West Suffolk Hospital | Bury St Edmunds, Suffolk, United Kingdom | Recruiting |
| Royal United Hospital | Bath, United Kingdom | Recruiting |
| Queen Elizabeth Hospital Birmingham | Birmingham, United Kingdom | Recruiting |
| The Royal Bournemouth Hospital | Bournemouth, United Kingdom | Recruiting |
| Fairfield General Hospital | Bury, United Kingdom | Recruiting |
| Addenbrooke's Hospital | Cambridge, United Kingdom | Recruiting |
| Kent and Canterbury Hospital | Canterbury, United Kingdom | Not Yet Recruiting |
| Countess of Chester Hospital | Chester, United Kingdom | Recruiting |
| Whiston Hospital | Liverpool, United Kingdom | Recruiting |
| Northwick Park Hospital | London, United Kingdom | Recruiting |
| King's College Hospital | London, United Kingdom | Recruiting |
| Milton Keynes University Hospital | Milton Keynes, United Kingdom | Recruiting |
+ 6 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT05476913