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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 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

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00021656
Enrollment
435
Registered
2020-05-18
Start date
2020-06-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tracking of the transport monitoring system

Interventions

Group 1: Investigation of efficiency and patient safety during patient transport using the Dräger monitoring system Group 2: Investigation of efficiency and patient safety during patient transport usi

Sponsors

Klinik für AnästhesiologieUniversitätsklinikum Heidelberg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients: - 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 Employees: - 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

Exclusion criteria: Patients: - 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 Employees: - Refusal to participate in the study - Non-compliance with the inclusion criteria

Design outcomes

Primary

MeasureTime frame
Clinical adverse events: Cardiopulmonary resuscitation, change of vital parameters requiring rapid intervention by the transport team, bradycardia, tachycardia, desaturation, dislocation of the intubation tube, dislocation of Respiratory cannula after tracheotomy, hypertension, hypotension, hypothermia, arrhythmias, unplanned admission to ICU

Secondary

MeasureTime frame
Efficiency: Transport time, rewiring, waiting time for bed, waiting time for equipment Usefulness: USE score, questions about cleaning and handling during intrahospital transport

Countries

Germany

Contacts

Public ContactFelix Schmitt

Klinik für Anästhesiologie, Universitätsklinikum Heidelberg

felix.schmitt@med.uni-heidelberg.de062215639421

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026