Stomach
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients who undergo upper gastrointestinal endoscopy. 2.The patients whose ECOG performance statues should be 0 or 1. 3.Patients who were over 20 years. 4.Patients who were eligible to this study criteria with written informed consent signed and dated.
Exclusion criteria
Exclusion criteria: 1.Patients who have risk factor of bleeding. 2.Patients who have history of distal or gastorectomy. 3.Patients with serious underlying disease. 4.Patients who are not eligible to this study due to psychotic disease or psychological symptoms. 5.Patients whom doctor decide not to register to this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of this study is to evaluate the safety of inflating a pressure of 20mmHg into the stomach during upper gastrointestinal endoscopy. | — |
Countries
Japan
Contacts
Fukuoka University Chikushi Hospital Department of Endoscopy