Clinical Trials Directory

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

TypeNameDescription
OTHERModified Fasting Groupa new fasting protocol is applied to subjects.
OTHERConventional Fasting Groupa 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.