ClinicalTrials.Veeva

Menu

Application of Simethicone in Esophagogastroscopy

A

Affiliated Hospital to Academy of Military Medical Sciences

Status

Completed

Conditions

Gastric Disease

Treatments

Other: Simethicone administration 20-30 min before the procedure
Other: Simethicone administration > 60 min before the procedure
Other: Simethicone administration 31-60 min before the procedure

Study type

Interventional

Funder types

Other

Identifiers

NCT03776916
307-simethicone

Details and patient eligibility

About

This is a randomized controlled trial to comparing the different simethicone administration strategies for esophagogastroscopy. Recent studies have indicated that the administration of simethicone before endoscopic examination could shorten the procedure time and improve the diagnostic rate of the gastric mucosal lesions. But the time interval between simethicone administration and the examination has not been fully determined. This study will test whether the time of taking simethicone before endoscopy could influence the performance of the procedure in a randomized controlled trial. The results may benefit the current clinical practice.

Full description

Esophagogastroscopy can enable the direct examination of the esophageal and gastric mucosal lesions, which has been widely applied in clinical practice. However, during the examination, too much water, foam or residues in the stomach will not only increase the procedure time and the misdiagnosis rate, but also decrease the patients' tolerance, for more efforts should be made to deal with the excessive water, foam or residues in order to obtain a clear view of the mucosa. Simethicone is also called poly-dimethylsiloxane, which can be used to remove the foam and water. Although simethicone has been routinely administrated before the esophagogastroscopy, the optimal strategy of administrating simethicone has not been clearly investigated, especially the time to administrate simethicone. Intaking simethicone too early will result in too excessive water in the stomach, while if the patients take it too late it doesn't take effects. Thus, this is a study to determine whether selecting different simethicone administration strategies could improve the performance of the esophagogastroscopy and minimize the patients' dissatisfaction.

Enrollment

311 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Above 18 years old patients
  • Who agree to participate in the study
  • Patients with the indications for gastroduodenoscopy

Exclusion criteria

  • Patients, who were receiving nonsteroidal anti-inflammatory drugs, pump inhibitors (PPI) or antibiotics in the last 3 weeks.
  • Severe uncontrolled coagulopathy
  • Prior history of gastric surgery.
  • Pregnancy and lactation

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

311 participants in 3 patient groups

Group 1
Experimental group
Description:
Simethicone administration 20-30 min before the procedure: Patients intake simethicone solution 20-30 min before the procedure.
Treatment:
Other: Simethicone administration 20-30 min before the procedure
Group 2
Experimental group
Description:
Simethicone administration 31-60 min before the procedure: Patients intake simethicone solution 31-60 min before the procedure.
Treatment:
Other: Simethicone administration 31-60 min before the procedure
Group 3
Experimental group
Description:
Simethicone administration \>60 min before the procedure; Patients intake simethicone solution \>60 min before the procedure.
Treatment:
Other: Simethicone administration > 60 min before the procedure

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems