Effectiveness of an Observational Unit at St. Olavs Hospital
NCT ID: NCT01092234
Last Updated: 2017-10-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
105 participants
INTERVENTIONAL
2010-03-31
2011-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
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Traditional ward
Traditional ward
provision of care in a traditional unit/ward.
Observational unit
Organizational change. Innovative organization of in-hospital care
Organizational change
Observational unit (new organizational unit) for organizing in-hospital care
Interventions
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Traditional ward
provision of care in a traditional unit/ward.
Organizational change
Observational unit (new organizational unit) for organizing in-hospital care
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* All patients on the list (appendix 1) with a tentative length of stay \< 24 hours
* Predicted stay of less than 24 hours
* Willingness and able to sign a informed consent
Exclusion Criteria
* Patients with a tentative length of stay \> 24 hours based on the summary of medical and logistical considerations e.g. need of major - surgery, infections with prolonged infusions of antibiotics.
* Unwillingness to sign a informed consent
* By discretion of the physician/surgeon
* Readmission of any reason in the study period (within 30 days)
18 Years
ALL
No
Sponsors
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St. Olavs Hospital
OTHER
Responsible Party
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Principal Investigators
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Erik Rødevand, MD
Role: PRINCIPAL_INVESTIGATOR
St. Olavs Hospital
Siv Mørkved, Professor
Role: STUDY_CHAIR
St. Olavs Hospital
Locations
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St. Olavs Hospital
Trondheim, , Norway
Countries
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Other Identifiers
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NO883974832
Identifier Type: OTHER
Identifier Source: secondary_id
2010/105-02
Identifier Type: -
Identifier Source: org_study_id