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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Completed |
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N/A | |
Completed |
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N/A | |
Completed |
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N/A | |
Completed |
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Phase 1 | |
Completed |
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Completed |
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N/A | |
Completed |
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The Effect of Oral Carbohydrate Solution on Anxiety and Comfort in Patients Undergoing Hip Arthroplasty
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N/A | |
Completed |
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Long-term Fasting: Multi-system Adaptations in Humans
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N/A | |
Recruiting |
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Recommended Clear Fluid Intake Volume at 2 Hours Prior to Esophagogastroduodenoscopy for Adult Patients
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N/A | |
Enrolling by invitation |
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N/A | |
Recruiting |
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Effect of Premedicant Oral Paracetamol on Gastric Volume and pH
|
Phase 4 | |
Not yet recruiting |
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Pre-Procedural Fasting in Cardiac Intervention
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N/A | |
Completed |
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Does Oral Intake Decreases Postoperative Pain Score in Children
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N/A | |
Completed |
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Short-Term Fasting During Chemotherapy in Patients With Gynecological Cancer- a Randomized Controlled Cross-over Trial
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N/A | |
Completed |
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Satiety Effects on the Neural Valuation of Food
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N/A | |
Completed |
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Phase 1 | |
Completed |
NCT01746719 -
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|
Phase 1 | |
Completed |
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Bioequivalence Study of Lisinopril and Hydrochlorothiazide Tablets (20+25) mg Under Fasting Conditions
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Phase 1 |