DRKS00021656Not yet recruitingNot 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 enrollmentStarted: May 18, 2020Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 435
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18 Years to one (—)
- Sex
- All
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
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