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

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.

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

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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