- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03724565
Air Quality Check in Gastrointestinal Endoscopy Unit
May 21, 2020 updated by: Chang Seok Bang, Chuncheon Sacred Heart Hospital
Air Quality Check in Gastrointestinal Endoscopy Unit Using Air Quality Monitoring Sensors
Air pollution sources in indoor area are one of the main factors for reducing indoor air quality of locations.
A gastrointestinal endoscopy unit consists of the following area: procedural, recovery areas, and area for a disinfection and cleaning for equipment.
This area is frequently exposed to the gastrointestinal gas expelled from patients and gas from electrocoagulated tissue through carbonation or electrocoagulation of neoplasms.
This can be potential harmful component for respiratory health not only to medical practitioners but also to the patients who undergo endoscopic examinations.
However, there has been scare data for the air quality check in the endoscopic unit.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Air pollution sources in indoor area are one of the main factors for reducing indoor air quality of locations.
A gastrointestinal endoscopy unit consists of the following area: procedural, recovery areas, and area for a disinfection and cleaning for equipment.
This area is frequently exposed to the gastrointestinal gas expelled from patients and gas from electrocoagulated tissue through carbonation or electrocoagulation of neoplasms (procedure of endoscopic submucosal dissection, endoscopic mucosal resection, etc).
This can be potential harmful component for respiratory health not only to medical practitioners but also to the patients who undergo endoscopic examinations.
However, there has been scare data for the air quality check in the endoscopic unit.
The aim of this study is to check the air quality using conventional portable passive air quality monitoring sensors in gastrointestinal endoscopy unit.
Study Type
Observational
Enrollment (Actual)
4320
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
-
-
Gangwon-do
-
Chuncheon, Gangwon-do, Korea, Republic of, 24253
- Chuncheon Sacred Heart Hospital
-
-
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
This study will check the only air quality in endoscopic unit of Hallym University Chuncheon Sacred Heart hospital of Korea, not a patients.
Description
Inclusion Criteria:
- This study will check the only air quality in endoscopic unit of Hallym University Chuncheon Sacred Heart hospital of Korea, not a patients.
Exclusion Criteria:
- This study will check the only air quality in endoscopic unit of Hallym University Chuncheon Sacred Heart hospital of Korea, not a patients.
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 |
---|---|
Endoscopic procedural area
air quality check of endoscopic procedural room
|
Air quality according to the method of endoscopic procedure will be checked (for example, upper diagnostic endoscopy, colonoscopy, endoscopic submucosal dissection, endoscopic mucosal resection, etc)
|
Recovery area for patients
air quality check of recovery area for patients in endoscopic unit
|
|
Cleansing area for equipments
air quality check of cleansing area for equipments in endoscopic unit
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
atmospheric Carbon dioxide (CO2)
Time Frame: up to 1 week
|
CO2 ppb level in the area of endoscopic unit
|
up to 1 week
|
atmospheric total volatile organic compound (TVOC)
Time Frame: up to 1 week
|
TVOC ppb level in the area of endoscopic unit
|
up to 1 week
|
atmospheric particulate matter that have a diameter of less than 2.5 micrometer (PM2.5)
Time Frame: up to 1 week
|
PM2.5 ug/m3 level in the area of endoscopic unit
|
up to 1 week
|
atmospheric nitrogen dioxide (NO2)
Time Frame: up to 1 week
|
NO2 ppb level in the area of endoscopic unit
|
up to 1 week
|
atmospheric carbon mono-oxide (CO)
Time Frame: up to 1 week
|
CO ppb level in the area of endoscopic unit
|
up to 1 week
|
atmospheric ozone
Time Frame: up to 1 week
|
ozone ppb level in the area of endoscopic unit
|
up to 1 week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
atmospheric temperature
Time Frame: up to 1 week
|
atmospheric temperature in the area of endoscopic unit
|
up to 1 week
|
atmospheric humidity
Time Frame: up to 1 week
|
atmospheric humidity in the area of endoscopic unit
|
up to 1 week
|
atmospheric pressure
Time Frame: up to 1 week
|
atmospheric pressure in the area of endoscopic unit
|
up to 1 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Chang Seok Bang, MD, PhD, Hallym University College of Medicine, Korea
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Actual)
June 17, 2018
Primary Completion (Actual)
November 17, 2018
Study Completion (Actual)
July 17, 2019
Study Registration Dates
First Submitted
October 27, 2018
First Submitted That Met QC Criteria
October 27, 2018
First Posted (Actual)
October 30, 2018
Study Record Updates
Last Update Posted (Actual)
May 21, 2020
Last Update Submitted That Met QC Criteria
May 21, 2020
Last Verified
May 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- bangairquality
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
There will be no patients-related data in this study (ecologic study)
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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