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Clinical Trials/NCT01718132
NCT01718132CompletedNot Applicable

Reduction of Postoperative Pain, Nausea and Vomiting

Triemli Hospital1 site in 1 country16,309 target enrollmentStarted: January 2009Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
16,309
Locations
1
Primary Endpoint
Pain
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Aim of this prospective study was to assess the quality of postoperative care in a postoperative anaesthesia care unit (PACU) using postoperative pain, nausea and vomiting as well as their reduction as quality markers. So far, only sparse data related to this topic are available and there are currently no established quality markers of a PACU service.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •All patients that have been transferred to the postanesthesia care unit postoperatively

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Pain

Secondary Outcomes

  • Postoperative nausea and vomiting

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Christoph K Hofer

Prof. Dr. med.

Triemli Hospital

Study Sites (1)

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