- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05686031
An Evaluation of Operating Room Staff's Awareness of Environmental Sustainability and Medical Waste Management
July 25, 2023 updated by: CIGDEM YILDIRIM GUCLU, Ankara University
The main goals of this single-centre cross-sectional study were to measure views on the environmental effects of the operating room and identify the main barriers to recycling in the operating room environment as perceived by the staff.
Participants responded a questionnaire to measure their opinions and the views.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
140
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
-
-
Çankaya
-
Ankara, Çankaya, Turkey
- AnkaraU
-
-
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
Sampling Method
Non-Probability Sample
Study Population
Anaesthesiologists, surgeons, residents, nurses, cleaning staff and medical students from any gender and age group working in Ankara University.
Description
Inclusion Criteria:
- all personel working in operating room
Exclusion Criteria:
- missing data
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
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Doctors
Anaesthesiologists
|
No interventions were done between groups
|
|
Anaesthesia Nurses
|
No interventions were done between groups
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Most reported barriers to recycling
Time Frame: 3 Weeks
|
3 Weeks
|
|
Views on the environmental effects of the OR
Time Frame: 3 Weeks
|
3 Weeks
|
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 (Actual)
October 14, 2019
Primary Completion (Actual)
November 4, 2019
Study Completion (Actual)
November 28, 2019
Study Registration Dates
First Submitted
January 6, 2023
First Submitted That Met QC Criteria
January 6, 2023
First Posted (Actual)
January 17, 2023
Study Record Updates
Last Update Posted (Actual)
July 27, 2023
Last Update Submitted That Met QC Criteria
July 25, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- I4-165-19
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
There is no intention and approval to share IPD
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.