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Improve the Comfort, Safety and Quality of Upper Endoscopy by a Modified Fasting Protocol

NCT05219136 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2022-06-01

No results posted yet for this study

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

  • Gastroscopy
  • Feelings
  • Fasting

Interventions

OTHER

Modified Fasting Group

a new fasting protocol is applied to subjects.

OTHER

Conventional Fasting Group

a conventional fasting protocol is applied to subjects.

Sponsors & Collaborators

  • The Affiliated Traditional Chinese Medicine Hospital Of Southwest Medical University

    collaborator UNKNOWN

  • Changhai Hospital

    lead OTHER

Principal Investigators

  • Lei Xin, Dr · Changhai Hospital

  • Luo-wei Wang, PhD · Changhai Hospital

  • Li Li, Dr · The Affiliated Traditional Chinese Medicine Hospital Of Southwest Medical University

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-10-07
Primary Completion
2021-12-31
Completion
2021-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05219136 on ClinicalTrials.gov