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The PROTECT Trial: PROpofol Titration to Enhance haemodynamiC sTability

Abroad (travel likely)Recruiting

Conditions

Anesthesia

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

  • Kantonsspital Baden, Baden, Switzerland

    Contact: Study coordinator (Andrea Kopp Lugl, PD Dr. med.) · andrea.kopplugli@ksb.ch · +41 56 486 13 60
    Contact: Principal Investigator (Andrea Kopp Lugl, PD Dr. med.)

  • University Hospital Basel, Basel, Switzerland

    Contact: Study coordinator (Martin Lohri, Dr. med.) · martindominik.lohri@usb.ch · +41 61 556 52 27
    Contact: Principal Investigator (Salome Dell-Kuster, Prof. Dr. med)
    Contact: Principal Investigator (Martin Lohri, Dr. med.)
    Nuno V. Gomes, Dr. med. (Sub-investigator)
    Funk Simon, Pract. med. (Sub-investigator)

  • Cantonal Hospital Graubünden, Chur, Switzerland

    Contact: Study coordinator (Martin Schläpfer, Prof. Dr. med.) · martin.schlaepfer@ksgr.ch · +41 81 256 65 05
    Contact: Principal Investigator (Martin Schläpfer, Prof. Dr. med.)

  • Kantonsspital Olten, soH, Olten, Switzerland

    Contact: Study coordinator (Kristian Mnich, Dr. med.) · kristian.mnich@spital.so.ch · +41 56 486 13 60
    Contact: Principal Investigator (Kristian Mnich, Dr. med.)
Study leads

  • Salome Dell-Kuster, Prof. Dr. med

    Principal Investigator

    University Hospital, Basel, Switzerland

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