Prospective evaluation for Propofol sedation in screening endoscopy
Not Applicable
Completed
- Conditions
- Healthy people
- Registration Number
- JPRN-UMIN000040330
- Lead Sponsor
- Sendai City Medical Center
- Brief Summary
Of 2305 eligible participants, no severe adverse effects nor accidents were reported. Eighty-six percent of the participants replied to hope to receive similar sedation in future endoscopy.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 2305
Inclusion Criteria
Not provided
Exclusion Criteria
no written consent
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Safety of propofol sedation
- Secondary Outcome Measures
Name Time Method