COVID-19
Conditions
Interventions
None listed
Sponsors
Oita San-ai Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who undergo endoscopy during the study period. Patients who agree the informed consent.
Exclusion criteria
Exclusion criteria: Patients who do not agree the informed consent. Patients who can not complete the examination due to body movement or respiratory deterioration.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the change of aerosol particle number at each time phase before, during, and after endoscopy and compare the trend of change of aerosol number in the situation of endoscopy and control group. | — |
Secondary
| Measure | Time frame |
|---|---|
| To analyze the relevance between patient characteristics, procedure related factors and increase or decrease of aerosol particles during endoscopy | — |
Countries
Japan
Contacts
Public ContactRyota Sagami
Oita San-ai Medical Center Department of Gastroenterology
Outcome results
None listed