How do Patients, Nurses and Physicians Perceive Negative Postoperative Events?
Perception of Surgical Complications - Agreements Among Patients, Nurses and Physicians
1 other identifier
observational
615
1 country
1
Brief Summary
The purpose of this study is to assess how patients, nurses and physicians perceive negative events following surgical procedures.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2009
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 4, 2008
CompletedFirst Posted
Study publicly available on registry
November 5, 2008
CompletedStudy Start
First participant enrolled
January 1, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2009
CompletedFebruary 10, 2015
February 1, 2015
11 months
November 4, 2008
February 9, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
To assess how patients, nurses and physicians perceive negative events following surgical procedures
August 2008- December 2009
Secondary Outcomes (1)
Association to the Clavien Dindo Classification
August 2008 - December 2009
Study Arms (3)
Patients
Patients who admit for a minor or major surgical intervention
Nurses
Medical staff of the University Hospital of Zurich
Physicians
Medical staff of the University Hospital of Zurich and other institutions
Interventions
Questionnaire, complications, grading severity, visual analog scale
Eligibility Criteria
Patients who will admit for a minor or major surgical procedure Nurses from the University Hospital of Zurich Different physicians of the University Hospital of Zurich (surgeons, anesthesia, urologist ans ICU-care specialists)and other institutions.
You may qualify if:
- Age: ≥ 18 years
- Capacity to act and no legal guardian
- Patients with any underlying disease admitted to the Department of Visceral and Transplantation Surgery of the University Hospital of Zurich with planned minor or major visceral surgery
- German language as daily language.
You may not qualify if:
- Patients with cognitive difficulties and diseases, which may yield unreliable answers
- Patients unable to read and write
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Visceral and Transplantation Surgery of the University Hospital of Zurich
Zurich, Canton of Zurich, 8091, Switzerland
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD PhD
Study Record Dates
First Submitted
November 4, 2008
First Posted
November 5, 2008
Study Start
January 1, 2009
Primary Completion
December 1, 2009
Study Completion
December 1, 2009
Last Updated
February 10, 2015
Record last verified: 2015-02