Individuals scheduled to undergo an upper gastrointestinal endoscopy
Conditions
Interventions
Oral Rehydration Jelly Intake
None
Sponsors
Suita Municipal Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Individuals aged 18 years or older who consent to participate in this study 2. Capable of oral intake 3. Individuals who, after receiving adequate explanation regarding participation in this trial, provided written consent based on full understanding and of their own free will
Exclusion criteria
Exclusion criteria: 1. Individuals with sodium or potassium intake restrictions 2. Individuals with severe liver disease, kidney disease, heart disease, or other conditions that make participation in this study difficult 3. Individuals with severe pharyngeal or nasal cavity conditions preventing endoscope insertion 4. Individuals in poor general health 5. Individuals requiring emergency endoscopy 6. Individuals undergoing endoscopy for hemostasis purposes 7. Individuals unable to independently decide on trial participation 8. Individuals who understand the trial but do not consent to participate 9. Other individuals deemed unsuitable for this study by the attending physician
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety of Upper Gastrointestinal Endoscopy | — |
Secondary
| Measure | Time frame |
|---|---|
| Vital signs before and after the examination (blood pressure, pulse rate, oxygen saturation), examination duration, level of hunger and stress prior to the examination, presence of any complications | — |
Countries
Japan
Contacts
Public Contactkoji Nagaike
Suita Municipal Hospital Endoscopy Center
Outcome results
None listed