A Prospective Single-center study on Pain Reduction by Peroral EGD Using an ultrathin Endoscope
Not Applicable
- Conditions
- Patients scheduled for upper gastrointestinal endoscopy
- Registration Number
- JPRN-UMIN000047366
- Lead Sponsor
- ihon University Hospital Gastroenterology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Patients who have refused to participate in this study (2) Patients who are considered by the investigator or sub-investigator as not suitable for participation in this study (3) Patients with serious cardiopulmonary diseases or coagulation disorders (4) Patients allergic to Xylocaine (5) Patients who cannot fill out the questionnaire by themselves (6) Patients who have undergone upper gastrointestinal tract surgery (7) Patients with known upper gastrointestinal lesions for which endoscopic or surgical treatment is planned.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Satisfaction compared to conventional diameter transoral upper gastrointestinal endoscopy
- Secondary Outcome Measures
Name Time Method Physician satisfaction with examination, examination time, biopsy site, time taken to biopsy, biopsy success rate, failure to diagnose by pathology, tumor detection rate, and primary endpoint results by skilled and unskilled physicians