DRKS00021656
Not yet recruiting
Not Applicable
Impact on clinical team experience and on patient preoperative care with intra-hospital transport, using 2 different vital sign monitoring solutions at a University Hospital. - IMPACT-Trial
Klinik für AnästhesiologieUniversitätsklinikum Heidelberg0 sites435 target enrollmentMay 18, 2020
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Tracking of the transport monitoring system
- Sponsor
- Klinik für AnästhesiologieUniversitätsklinikum Heidelberg
- Enrollment
- 435
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- Age: 18\+
- •\- informed consent
- •\- Inpatients admitted to hospital, including patients pre\-registered for surgery
- •\- Transports between the induction room, operating theatre, recovery room and intensive care unit and all transports between these units and departments for examinations (e.g. imaging)
- •\- Patients who are already in the clinic and need a re\-operation
- •\- age: 18\+
- •\- informed consent
- •\- Employees (doctors, nurses) of the Clinic for Anaesthesiology, at Heidelberg University Hospital, who are involved in the care of the above\-mentioned patients.
Exclusion Criteria
- •\- Patients out of the emergency room
- •\- Patients who are unable to give information
- •\- Patients with infections that require additional protective measures: o Cholera o Diphtheria o Haemorrhagic fever o Meningoencephalomyelitis (if the aetiology is unclear or caused by enteroviruses) o Query fever (syn. also Q fever, Queensland fever, Balkan flu) o Rabies o TB, also Koch's disease (if infectious) o Typhoid o Chickenpox o Generalized zoster
- •\- Patients from whom three transports have already been observed should not be included for further observations
- •\- Refusal to participate in the study
- •\- Non\-compliance with the inclusion criteria
Outcomes
Primary Outcomes
Not specified
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