The purpose of the study is to test the impact of the StOP?-protocol - an intra-operative communication briefing, on post-operative mortality and important patient outcomes.
The StOP?-protocol is a communication briefing initiated by the responsible surgeon during a surgical operation. The surgeon informs the team present in the operating room about the current Status of the operation, the Objectives of the next steps and the potential Problems the surgical team may meet; the responsible surgeon encourages the team to voice any question or concern (?). To test the impact of the StOP?-protocol on patient outcomes, the study is designed as a randomized controlled trial. Surgeons will be randomized either (a) in the intervention group and be trained to perform the StOP?-protocol or (b) in the control group and will communicate as they prefer during their operations. Post-operative patient outcomes of the surgeons in the intervention and the control group will be compared to evaluate the effects of the StOP?-protocol.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Enrollment
400
The StOP?-protocol is an intra-operative briefing initiated by the responsible surgeon. When performing a StOP?-protocol, the surgeons inform the team present in the operating room about the Status (St) of the operation, the Objectives (O) of the operations, the potential problems (P) they may meet and encourage the team to ask questions or voice concerns (?). The responsible surgeon announces at the team timeout when they plan to perform the StOP-protocol(s).
Tirol Kliniken GmbH
Innsbruck, Austria
RECRUITINGKantonsspital Baselland
Liestal, Basel-Landschaft, Switzerland
Mortality within 30 days after the operation
Mortality within 30 days after the operation in the intervention arm compared to the control arm
Time frame: 30 days after the index operation
Unplanned reoperations within 30 days after the operation
Unplanned reoperations within 30 days after the operation in the intervention arm compared to the control arm
Time frame: 30 days after the index operation
Length of hospital stay
Length of hospital stay in the intervention arm compared to the control arm
Time frame: It is reasonable to estimate that the information will be available after 60 post-operative days for most patients
Unplanned hospital readmissions within 30 days after the operation
Unplanned hospital readmissions within 30 days after the operation in the intervention arm compared to the control arm
Time frame: 30 days after the index operation
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Kantonsspital Baden AG
Baden, Canton of Aargau, Switzerland
ACTIVE_NOT_RECRUITINGBern University Hospital (Inselspital)
Bern, Canton of Bern, Switzerland
ACTIVE_NOT_RECRUITINGHôpital Fribourgeois
Fribourg, Canton of Fribourg, Switzerland
ACTIVE_NOT_RECRUITINGCentre Hospitalier Universitaire Vaudois (CHUV)
Lausanne, Canton of Vaud, Switzerland
ACTIVE_NOT_RECRUITINGSpital Limmattal
Schlieren, Canton of Zurich, Switzerland
ACTIVE_NOT_RECRUITINGKantonsspital Winterthur
Winterthur, Canton of Zurich, Switzerland
ACTIVE_NOT_RECRUITINGStadtspital Zürich Triemli
Zurich, Canton of Zurich, Switzerland
ACTIVE_NOT_RECRUITINGEOC Civico Lugano and EOC ospedale regionale di Bellinzona
Lugano, Canton Ticino, Switzerland
RECRUITING...and 3 more locations