Safe Brain Initiative, Operationalizing Precision Anaesthesia

NCT05765162 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 15000

Last updated 2024-06-07

No results posted yet for this study

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

  • Neurocognitive Disorders
  • Post Operative Delirium
  • Pain
  • Nausea
  • Vomiting
  • Wellbeing
  • Shivering
  • Anxiety
  • Stress
  • Agitation,Psychomotor
  • Sedation Complication
  • Thirst
  • Satisfaction, Patient
  • Temperature Change, Body
  • Fasting
  • Sore-throat
  • Hearing and Vision Loss

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

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05765162 on ClinicalTrials.gov