NCT00785096

Brief Summary

The purpose of this study is to assess how patients, nurses and physicians perceive negative events following surgical procedures.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
615

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2009

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 4, 2008

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 5, 2008

Completed
2 months until next milestone

Study Start

First participant enrolled

January 1, 2009

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2009

Completed
Last Updated

February 10, 2015

Status Verified

February 1, 2015

Enrollment Period

11 months

First QC Date

November 4, 2008

Last Update Submit

February 9, 2015

Conditions

Keywords

Perception, surgical complications, patients, nurses and physicians

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

Other: Questionnaire

Nurses

Medical staff of the University Hospital of Zurich

Other: Questionnaire

Physicians

Medical staff of the University Hospital of Zurich and other institutions

Other: Questionnaire

Interventions

Questionnaire, complications, grading severity, visual analog scale

NursesPatientsPhysicians

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

Location

MeSH Terms

Interventions

Surveys and Questionnaires

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

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

Locations