EuPrecho Study Flyer V1.1 25JJUN2024
EuPreCHO
European study on perioperative management and outcome following Preoperative Transthoracic Echocardiography in noncardiac surgery patients.
Dear collaborators and investigators,
Thank you for your interest in EuPreCHO study. If you are interested in participating, please complete the Call for the Centres form: Call for centres – ESAIC
ClinicalTrials.gov ID: NCT06409234
Chief Investigators
Prof. Dr. Giovanna Lurati Buse – University Hospital Düsseldorf, Germany
MSc & Prof. Michelle Chew, PhD- Linköping University Hospital, Sweden
Call for centres form
Steering committee
Fernando Abelha, MD, PhD- Porto, Portugal
Gareth Ackland, PhD FRCA FFICM-London, UK
Kateryna Bielka, MD, PhD, Kyiv, Ukraine
Bernardo Bollen-Pinto, MD, PhD, Geneva, Switzerland
Stefan De Hert, MD, PhD, Ghent, Belgium
Simon Howell MA(Cantab) MRCP FRCA MSc MD, Leeds, UK
Jean-Luc Fellahi, MD, PhD, Lyon, France
Katarzyna Kotfis MD, PhD, Szczecin, Poland
Jan Larmann MD, PhD, Heidelberg, Germany
Purificación Matute, MD, PhD, Barcelona, Spain
Ekatarina Popova, PhD, Barcelona, Spain
Christian Puelacher, MD,PhD, Innsbruck, Austria
Spadaro Savino, MD, PhD, Ferrara, Italy
Judith van Waes, MD PhD, Utrecht, The Netherlands
Prof Peter Zahn, MD PhD, Bochum, Germany
Daniela Ionescu, MD, Cluj Napoca, Romania
Malachy Columb, FRCA, FFICM, Manchester, UK
He Zhang, PhD Linköping, Sweden
Protocol, Appendices and other Study Documents
EuPreCHO – Study Synopsis V2.0 04SEP2024
EuPreCHO Protocol V1.0 04SEPT24
EuPreCHO Appendix 1A – Information sheet and Consent form V1.0 04SEPT24
EuPreCHO Appendix 1B – Information sheet and Consent form V1.0 04SEP2024
EuPreCHO Appendix 2 – Endpoint Definitions V1.0 04SEPT24
EuPreCHO Appendix 3 – Flowchart Study Assessment V1.0 04SEPT24
EuPreCHO Appendix 4- Screening Log V1.0 04SEPT24
EuPreCHO Appendix 5 – List of procedural risk of common procedures V1.0 04SEPT24
EuPreCHO Appendix 6 – Case Report Form V2. Dated 17APR2025
EuPreCHO Appendix 7 – End of study Reporting Form V1.0 04SEPT2024
Support Document- Approval Documentation Coversheet
Support Document-Part I OpenClinica Basic Instructions
Support Document-Part II Study Specific Instructions
EuPreCHO FAQ
Translations
WHODAS EuPreCHO
EuPreCHO – WHODAS V2.0 -English
EuPreCHO – WHODAS V2.0 -Spanish
EuPreCHO – WHODAS V2.0 -Croatian
EuPreCHO – WHODAS V2.0 -Dutch
EuPreCHO – WHODAS V2.0 -German
EuPreCHO – WHODAS V2.0 -Swedish
Austria- EuPreCHO
EuPreCHO Appendix 1B Information and consent form
Croatia- EuPreCHO
EuPreCHO Appendix 1B Information and consent form
Germany- EuPreCHO
EuPreCHO Appendix 1B Information and consent form
Greece- EuPreCHO
EuPreCHO Appendix 1A Information and consent form
EuPreCHO Appendix 1B Information and consent form
Italy- EuPreCHO
EuPreCHO Appendix 1A Information and consent form
EuPreCHO Appendix 1B Information and consent form
EuPreCHO Appendix 3 Flow Chart
EuPreCHO Protocol
Netherlands- EuPreCHO
EuPreCHO Appendix 1AInformation and consent form
Poland – EuPreCHO
EuPreCHO Appendix 1A Information and consent form
EuPreCHO Appendix 2 – Endpoint Definitions V1.0 04SEPT24
EuPreCHO Appendix 3 – Flowchart Study Assessment V1.0 04SEPT24
EuPreCHO Appendix 04 – Screening log V1.0 04SEPT24
EuPreCHO Appendix 5 – List of procedural risk of common procedures V1.0 04SEPT24
EuPreCHO Appendix 7 – End of study Reporting Form V1.0 04SEPT2024
Portugal – EuPreCHO
EuPreCHO Appendix 1A Information and consent form
EuPreCHO Appendix 1B Information and consent form
Romania – EuPreCHO
EuPreCHO Appendix 1A Information and consent form
Spain
EuPreCHO Appendix 1B Information and consent form
Switzerland
EuPreCHO Appendix 1B Information and consent form
Sponsor
The Study is entirely sponsored by a grant from the European Society of Anaesthesiology and Intensive Care Clinical Trial Network (ESAIC CTN). The ESAIC CTN provides an infrastructure for clinical research in the fields of Anaesthesia, Pain, Intensive Care and Emergency Medicine by transnational European collaborative studies.