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NCT01718132 Clinical Trial

Reduction of Postoperative Pain, Nausea and Vomiting

Post Operative Pain Clinical Trial

Official title:
Reduction of Postoperative Pain, Nausea and Vomiting

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01718132
Other study ID # AWR-2012-STZ
Secondary ID KEK-StV-Nr. 47/1
Status Completed
Phase N/A
First received October 27, 2012
Last updated October 30, 2012
Start date January 2009
Est. completion date June 2012

Study information
Verified date October 2012
Source Triemli Hospital
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 16309
Est. completion date June 2012
Est. primary completion date June 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

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

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Switzerland Triemli City Hospital Zurich

Sponsors (1)
Lead Sponsor Collaborator
Triemli Hospital

Country where clinical trial is conducted

Switzerland, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain
Secondary Postoperative nausea and vomiting
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