Prospective trial to safety of gastric pressure measurement
Not Applicable
Recruiting
- Conditions
- Stomach
- Registration Number
- JPRN-UMIN000039105
- Lead Sponsor
- Fukuoka University Chikushi Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
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.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint of this study is to evaluate the safety of inflating a pressure of 20mmHg into the stomach during upper gastrointestinal endoscopy.
- Secondary Outcome Measures
Name Time Method