- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01213069
Staff Opinions and Knowledge Concerning Organ and Tissue Harvesting: an Investigation Among the Patient Care Personnel in the South-Mediterranean Region of France
March 24, 2015 updated by: Centre Hospitalier Universitaire de Nīmes
The goal of this study is to evaluate the knowledge of paramedical and medical care personnel concerning organ and tissue donations, as well as their opinions on this activity.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
1859
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Marseille, France, 13915
- AP-HM Hôpital Nord
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Montpellier Cedex 05, France, 34295
- Hôpital Guy de Chauliac, CHU de Montpellier
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Nice, France, 06003
- Hôpital Cimiez, CHU de Nice
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Nimes, France, 30029
- Centre Hospitalier Universitaire de Nîmes
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Health care personnel in South-Mediterranean France
Description
Inclusion Criteria:
- paramedical or medical care personnel from a participating center
- participates in organ donor activities
- works in a department with organ donor activity
Exclusion Criteria:
- personnel with no contact with organ donor activities
- personnel from non-participating centers
- refuses to participate
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
all 5000 subjects
this is a purely descriptive study with one group
|
The subjects are asked to fill out a questionnaire on the personal and professional situations, organ donation legislation, what happens in everyday practice, their own experience with donating their own organs, and what position they take.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
VAS Negative/positive feeling
Time Frame: 1 day
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Visual Analog Scale from 0 to 100 where 0 is negative and 100 is positive.
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2010
Primary Completion (Actual)
July 1, 2012
Study Completion (Actual)
July 1, 2012
Study Registration Dates
First Submitted
September 30, 2010
First Submitted That Met QC Criteria
September 30, 2010
First Posted (Estimate)
October 1, 2010
Study Record Updates
Last Update Posted (Estimate)
March 25, 2015
Last Update Submitted That Met QC Criteria
March 24, 2015
Last Verified
March 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- PHRC-I/2009/CB-01
- 1391089 (Other Identifier: France: Commission Nationale de l'Informatique et des Libertés)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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