- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06210906
Gastric Volume Following Sips of Water Intake
February 13, 2024 updated by: Jin-Young Hwang, SMG-SNU Boramae Medical Center
Gastric Volume Following Sips of Water Intake Within 1 Hour in Preoperative Fasting Elderly Patients; Observational Study
We aim to observe whether drinking of sips of water within 1 hour before surgery significantly affects the gastric volume.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
200
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients over 65 years old undergoing elective surgery under general anesthesia
Description
Inclusion Criteria:
- Patients over 65 years old undergoing elective surgery under general anesthesia
Exclusion Criteria:
- History of gastric surgery
- Anatomical anomaly, diseases, or mass in the stomach
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Sips of water
Patients taking sips of water within 1 hour in preoperative fasting
|
Gastric volume is assessed using ultrasound.
|
|
No sips of water
Patients not taking sips of water within 1 hour in preoperative fasting
|
Gastric volume is assessed using ultrasound.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Gastric volume
Time Frame: Immediately before induction of anesthesia
|
Gastric volume is assessed using ultrasound in the supine and right lateral decubitus position.
|
Immediately before induction of anesthesia
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
February 26, 2024
Primary Completion (Estimated)
February 21, 2025
Study Completion (Estimated)
February 21, 2025
Study Registration Dates
First Submitted
January 8, 2024
First Submitted That Met QC Criteria
January 8, 2024
First Posted (Actual)
January 18, 2024
Study Record Updates
Last Update Posted (Estimated)
February 14, 2024
Last Update Submitted That Met QC Criteria
February 13, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2024-1
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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