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CompletedNCT05469633Updated Aug 14, 2024

Application of Portable Ultrasonic Evaluation of Gastric Contents in Painless Gastroscopy

An observational study in Ultrasound Evaluation of Gastric Contents, sponsored by The Second Affiliated Hospital of Chongqing Medical University. Completed at 1 site in China. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-08-14.

Sponsored by The Second Affiliated Hospital of Chongqing Medical University · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
600
Ages
18 Years and older
Sex
All
01

Study summary

To explore the correlation between gastric ultrasound evaluation and gastroscopic direct vision evaluation of gastric contents, so as to more accurately use gastric ultrasound to evaluate the gastric contents of patients undergoing painless electronic gastroscopy in the outpatient department, so as to develop an individual painless diagnosis and treatment strategy to reduce the risk of lung aspiration.

02

Conditions studied

  • Ultrasound Evaluation of Gastric Contents

Keywords

  • gastric ultrasound
  • gastric contents
  • painless electronic gastroscope
03

In context

Lead sponsor

The Second Affiliated Hospital of Chongqing Medical University is the lead sponsor of 98 studies on the registry; 29 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Outpatients undergoing painless electronic gastroscopy were fasted for 8 hours in acccordance with gastroscopy guidelines

Inclusion criteria

  • ≥18years
  • Patients undergoing painless electronic gastroscopy.
  • Voluntarily participate and sign informed consent.

Exclusion criteria

Exclusion Criteria:

  • Patients undergoing general electronic gastroscopy.
  • Patients who refused to undergo gastric ultrasound.
  • Patients with postural difficulties during gastric ultrasonography.
  • with fresh wounds or infections at the site of Gastric ultrasound
  • Patients whose ultrsound image quality is too poor to properly display the relevant anatomical structures.
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
600 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. The cross-sectional area of the antrum (CSA)

    The maximum anteroposterior diameter (recorded as D1) and maximum craniocaudal diameter (recorded as D2) between the gastric antrum serosal surfaces were measured perpendicularly to each other.CSA(cm2) = (π × D1 × D2) / 4

    Time frame: Before the painless electronic gastroscopy

  2. Predicted volume

    Predicted volume calculated by CSA

    Time frame: Before the painless electronic gastroscopy

  3. Observed volume

    All gastric fluid was thoroughly suctioned through an endoscope side port, measured to the nearest mL and recorded

    Time frame: Before the painless electronic gastroscopy

07

Study locations

1 site
  • The Second Affiliated Hospital, Chongqing Medical University
    Chongqing, Chongqing 400010, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 14, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05469633
Lead sponsor
The Second Affiliated Hospital of Chongqing Medical University
Responsible party
Sponsor
First posted
Jul 22, 2022
Start date
Aug 29, 2022
Primary completion
Jul 31, 2023
Completion
Jul 31, 2023
Last update
Aug 14, 2024

Study contacts

Chen Yupei
study director · Department of Anesthesiology,The Second Affiliated Hospital ,Chongqing Medical University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2022. You cannot join it, but the record below documents what was studied.

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