- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04124562
Nitrous Oxide Frequency of Use and Causes in Hospital in Turkey
January 25, 2020 updated by: Hilmi Demirkiran, MD, Yuzuncu Yıl University
The prevalence of nitrous oxide use in hospitals in Turkey
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Nitrous oxide has a long history of use in the healthcare field for over 150 years.
However, this gas is slowly being abandoned for various reasons.
The decrease in N2O use is probably due to its side effects and negative impact on global warming.
Proven side effects include irreversible toxic effects on bone marrow, relative or absolute contraindications related to neuro and cardiac anesthesia, increased incidence of post-operative nausea and vomiting, increased risk of miscarriage in pregnant women (5), the greenhouse effect of nitrous oxide.
In 2013, B. Husum et al. investigated the frequency of N2O use in public hospitals in Scandinavian countries and it was confirmed that N2O use was reduced and limited.
According to the results of this research, N2O was administered with a volatile anesthetic agent in 21.5% of general anesthesia applications in Scandinavian countries.
N2O was used as the second agent in Denmark by 2.4%, Finland by 17%, Iceland by 34.5, Norway by 32.1%, Sweden by 27.5%.
In Turkey there are not enough reports of N2O use prevalence.
In this study, we will investigate the extent of use and avoidance reasons N2O in Turkey.
And we aim creating awareness.
Study Type
Observational
Enrollment (Actual)
170
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
-
-
Tusba / Zeve Kampus
-
Van, Tusba / Zeve Kampus, Turkey, 65080
- Yuzuncu Yil University, School of Medicine
-
-
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
N/A
Sampling Method
Non-Probability Sample
Study Population
Anesthesiologists working in the operating rooms of hospitals in Turkey
Description
Inclusion Criteria:
Hospitals who accept to participate in Turkey
-
Exclusion Criteria:
Hospitals refusing to participate in the study
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 percentage of nitrogen oxide use
Time Frame: A day
|
Percentage of nitrogen oxide use in a daily general anesthesia practice
|
A day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The percentage of nitrogen oxide use
Time Frame: A month
|
Percentage of nitrogen oxide use in a monthly general anesthesia practice
|
A month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Hilmi Demirkıran, 1, Study Director
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 (Actual)
October 15, 2019
Primary Completion (Actual)
November 15, 2019
Study Completion (Actual)
November 15, 2019
Study Registration Dates
First Submitted
October 8, 2019
First Submitted That Met QC Criteria
October 10, 2019
First Posted (Actual)
October 11, 2019
Study Record Updates
Last Update Posted (Actual)
January 28, 2020
Last Update Submitted That Met QC Criteria
January 25, 2020
Last Verified
January 1, 2020
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Nitrous oxide
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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