Trials / Completed
CompletedNCT05219136
Improve the Comfort, Safety and Quality of Upper Endoscopy by a Modified Fasting Protocol
Improve the Comfort, Safety and Quality of Upper Endoscopy by a Modified Fasting Protocol:a Double-center, Prospective, Controlled Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 200 (actual)
- Sponsor
- Changhai Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
This double-center, prospective, interventional study aims to include 200 gastroscopic procedures and investigate the relationship between fasting time and feeling of subjects. The subjects will all receive examination between 10:30 to 11:30am. In the control group, the subjects are required to start the fast at 10:00pm the day before examination and can not drink water after 8:00am on the day of examination. In the test group, the subjects are required to have customized rice congee before 6:30am on the examination day and can not drink water after 8:00am. All subjects complete questionnaire which include discomfort and willingness to accept the same fasting regimen.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Modified Fasting Group | a new fasting protocol is applied to subjects. |
| OTHER | Conventional Fasting Group | a conventional fasting protocol is applied to subjects. |
Timeline
- Start date
- 2021-10-07
- Primary completion
- 2021-12-31
- Completion
- 2021-12-31
- First posted
- 2022-02-01
- Last updated
- 2022-06-01
Locations
2 sites across 1 country: China
Source: ClinicalTrials.gov record NCT05219136. Inclusion in this directory is not an endorsement.