- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02199535
The Analysis of the Risks of the Personnel Working in Anesthesiology Departments in Turkey
November 4, 2014 updated by: Dilek Günay CANPOLAT, TC Erciyes University
The aim of the study was to investigate the analysis of the risks faced by the personnel working in the field of Anesthesiology and Reanimation in Turkey
Study Overview
Status
Completed
Conditions
Detailed Description
There are many potential risks in operating room such as anesthetic gas exposure, chronic noise, fair, intensive working conditions, frequent guardians of the doctors and anesthesia staff.
Those are effects the staff of anesthesia such as doctors, anesthesia assistants, anesthesia nurses.
They usually suffer from hard working, fatigue and exposing anesthetic gases effects them as well.
These reasons cause some undesirable adverse effects.
The scientific dates are really limited in uour country.
We aimed to ask questions the anesthesia staff and determine the environment conditions and the other risk in operating room that effects the staff.
For t his purpose we prepared a questionaire and send to their e-mail address.
Study Type
Observational
Enrollment (Actual)
568
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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Kayseri, Turkey, 38039
- Erciyes University
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
The anesthesia staff doctors nurses and anesthesia personal
Description
Inclusion Criteria:
- anesthesia doctors anesthesia nurses anesthesia technic personal
Exclusion Criteria:
-
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The analysis of the risks in the operating room
Time Frame: during 1 months
|
This a questionnaire study.
We prepared a questionnaire and send it to anesthesia staff by e-mail address.
their reply will evaluated
|
during 1 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
August 1, 2014
Primary Completion (Actual)
November 1, 2014
Study Completion (Actual)
November 1, 2014
Study Registration Dates
First Submitted
July 22, 2014
First Submitted That Met QC Criteria
July 23, 2014
First Posted (Estimate)
July 24, 2014
Study Record Updates
Last Update Posted (Estimate)
November 5, 2014
Last Update Submitted That Met QC Criteria
November 4, 2014
Last Verified
November 1, 2014
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2014/340
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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