Survey of Pain and Incidentalities Associated with Upper Gastrointestinal Endoscopy

Survey of Pain and Incidentalities Associated with Upper Gastrointestinal Endoscopy - Survey of Pain and Incidentalities Associated with Upper Gastrointestinal Endoscopy

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000056639

Enrollment

1000

Registered

2025-01-06

Start date

2025-01-06

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Upper Gastrointestinal Endoscopy

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Those who have undergone a narrow upper gastrointestinal endoscopy at Harusaki Health Screening Center as part of a physical checkup or gastric cancer screening

Exclusion criteria

Exclusion criteria: Persons who cannot give consent to participate in research

Design outcomes

Primary

Measure	Time frame
A questionnaire survey (an observational study) will be conducted for the purpose of investigating the incidentalities associated with narrow upper gastrointestinal endoscopy. The principal investigator will explain the study to all consecutive patients who have undergone the examination, and will give the questionnaire to those who have confirmed their willingness to participate in the study. The research subjects will describe and submit a description of the degree of pain before and after the examination immediately after the examination. The research subjects will be observed for symptoms for up to one week thereafter, and if there is a contingency event, they will self-administer the symptoms, their degree and duration of occurrence on the questionnaire, and return it to the research office by mail.	—

Measure

Time frame

A questionnaire survey (an observational study) will be conducted for the purpose of investigating the incidentalities associated with narrow upper gastrointestinal endoscopy. The principal investigator will explain the study to all consecutive patients who have undergone the examination, and will give the questionnaire to those who have confirmed their willingness to participate in the study. The research subjects will describe and submit a description of the degree of pain before and after the examination immediately after the examination. The research subjects will be observed for symptoms for up to one week thereafter, and if there is a contingency event, they will self-administer the symptoms, their degree and duration of occurrence on the questionnaire, and return it to the research office by mail.

—

Countries

Japan

Contacts

Public ContactTSUNEYA WADA

Okazaki City Medical Association Harusaki Medical check Center

wadat0123@yahoo.co.jp+81-564-52-1572

Outcome results