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GEKO Venous Thromboembolism Prevention Study

Abroad (travel likely)Recruiting

Conditions

Stroke, Acute · Venous Thromboembolism · Deep Vein Thrombosis · Pulmonary Embolism

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations

  • West Suffolk Hospital, Bury St Edmunds, Suffolk, United Kingdom

    Contact: Study coordinator (Lisa Wood)
    Contact: Study coordinator (Catherine Durrant)
    Contact: Principal Investigator (Abul Azim, Dr)

  • Royal United Hospital, Bath, United Kingdom

    Contact: Study coordinator (Hayley Stoney) · ruh-tr.StrokeResearch@nhs.net
    Contact: Study coordinator (Telma Costa)
    Contact: Principal Investigator (Andrew Stone, Dr)

  • Queen Elizabeth Hospital Birmingham, Birmingham, United Kingdom

    Contact: Study coordinator (Scott Luxmore-Brown)
    Contact: Principal Investigator (Mark Willmot, Dr)

  • The Royal Bournemouth Hospital, Bournemouth, United Kingdom

    Contact: Study coordinator (Dhanya Babu) · +44(0)300 019 5073
    Contact: Principal Investigator (Kamy Thavanesan, Dr)

  • Fairfield General Hospital, Bury, United Kingdom

    Contact: Study coordinator (Pamela Bradley)
    Contact: Principal Investigator (Narayanamoorthi Saravanan, Dr)

  • Addenbrooke's Hospital, Cambridge, United Kingdom

    Contact: Study coordinator (Alex McGovern)
    Contact: Principal Investigator (Smriti Agarwal, Dr)

  • Kent and Canterbury Hospital, Canterbury, United Kingdom

    Contact: Study coordinator (Gemma Hector)
    Contact: Principal Investigator (Rami Abdallah, Dr)

  • Countess of Chester Hospital, Chester, United Kingdom

    Contact: Study coordinator (Sherin Sabu)
    Contact: Principal Investigator (Kausik Chatterjee, Dr)

  • Whiston Hospital, Liverpool, United Kingdom

    Contact: Study coordinator (Coleen Ditchfield)
    Contact: Principal Investigator (Sunanda Mavinamane, Dr)

  • Northwick Park Hospital, London, United Kingdom

    Contact: Study coordinator (Parvathy Gopi) · +44(0)2088695550
    Contact: Principal Investigator (Aravinth Sivagnanaratnam, Dr)

  • King's College Hospital, London, United Kingdom

    Contact: Study coordinator (Con Tibajia) · +44(0)2032997506
    Contact: Principal Investigator (Yee-Haur Mah, Dr)

  • Milton Keynes University Hospital, Milton Keynes, United Kingdom

    Contact: Study coordinator (Cheryl Padilla-Harris)
    Contact: Principal Investigator (Yaw Duodu, Dr)

  • Queen's Medical Centre, Nottingham, United Kingdom

    Contact: Study coordinator (Amanda Hedstrom) · +44(0)1158231807
    Contact: Principal Investigator (Ashit Shetty, Dr)

  • Salford Royal Hospital, Salford, United Kingdom

    Contact: Study coordinator (Reece Doonan) · +44(0)161 206 2188
    Contact: Principal Investigator (Kirsty Ward, Dr)

  • Stepping Hill Hospital, Stockport, United Kingdom

    Contact: Study coordinator (Seethalekshmi Vikramadhithyan) · +44(0)161 419 5893
    Contact: Study coordinator (Clare Tibke)
    Contact: Principal Investigator (Georgina Williams)

  • Royal Stoke University Hospital, Stoke-on-Trent, United Kingdom

    Contact: Study coordinator (Surabhi Saxena) · +44(0)1782671988
    Contact: Principal Investigator (Phillip Ferdinand, Dr)

  • New Cross Hospital, Wolverhampton, United Kingdom

    Contact: Study coordinator (Tegan Taylor) · +44(0)1902307999
    Contact: Principal Investigator (Nasar Ahmad, Dr)

  • Yeovil Hospital, Yeovil, United Kingdom

    Contact: Study coordinator (Alfonso Tanate) · +44(0)193538 4297
    Contact: Principal Investigator (Khalid Rashed, Dr)
Study leads

  • Christine Roffe, MD FRCP FESO

    Principal Investigator

    Keele University, University Hospitals of North Midlands NHS Trust

View source on ClinicalTrials.gov(opens in a new tab)