Fasting Clinical Trial
Official title:
Improve the Comfort, Safety and Quality of Upper Endoscopy by a Modified Fasting Protocol:a Double-center, Prospective, Controlled Study
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.
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Status | Clinical Trial | Phase | |
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Active, not recruiting |
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Phase 1 | |
Completed |
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Completed |
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N/A | |
Completed |
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Completed |
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Recruiting |
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N/A | |
Enrolling by invitation |
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N/A | |
Recruiting |
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Phase 4 | |
Not yet recruiting |
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N/A | |
Completed |
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Completed |
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Completed |
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Phase 1 | |
Completed |
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Phase 1 | |
Completed |
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Completed |
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Bioequivalence Study of Etodolac Capsules USP 300 mg Under Fasting Condition
|
Phase 1 |