Safe Brain Initiative, Operationalizing Precision Anaesthesia
NCT05765162 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 15000
Last updated 2024-06-07
Summary
Perioperatively, patients experience an unnecessarily high level of side effects associated with their treatment. These side effects include nausea, severe pain, anxiety, and stress. Moreover, many patients develop postoperative delirium (POD) and neurocognitive dysfunctions, often resulting in long-term cognitive impairment, decreased quality of life, and increased mortality. However, physicians, nurses and their institutions do not receive structured feedback regarding these aspects of each patient's well-being. They may therefore be unable to engage in the essential cause-and-effect learning necessary to evaluate and consecutively reduce such side effects.
Effective guidelines conform prevention is the proven key to shielding our patients from adverse Outcomes. The Safe Brain Initiative's high-quality routine data-for-action is a sword and accelerator for moving towards patient-centred, precision care. Thus, establishing a foundation for value-based and patient-centred healthcare development.
However, a turnkey real-world solution is challenging to develop and implement and requires substantial resources. As a result, such solutions are usually beyond the scope of a single institution. The SBI platform provides high-quality, real-world data to bridge this gap. It allows monitoring and in-depth analysis of cause and effect in the day-to-day routine of individuals, departments, and institutions.
The SBI's approach is continuously improved and updated. An organization called the SBI Global Society oversees the quality and precision of science through experts in the field. At SBI Hospitals and Flagship centres, Masterclasses are conducted and can be attended alongside clinical immersions.
SBI Solutions manages, develops, and provides technical and service support for the Safe Brain Initiative. Its service guarantees the professional and GDPR conform management of data handling and storage as well as the user-friendly functionality of the SBI-Dashboard solutions.
Conditions
Interventions
- BEHAVIORAL
-
Patient reported ourcomes
Full screening for the perioperative periode
Sponsors & Collaborators
-
Nykøbing Falster County Hospital
collaborator OTHER -
Ankara University
collaborator OTHER -
Naestved Hospital
collaborator OTHER -
University of Bern
collaborator OTHER -
University of Southern Denmark
lead OTHER
Principal Investigators
-
Finn M. Radtke, Professor · University of Southern Denmark
Eligibility
- Min Age
- 18 Years
- Max Age
- 100 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-12-01
- Primary Completion
- 2025-01-01
- Completion
- 2026-01-01
Countries
- Denmark
Study Locations
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