- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03567915
Ultrasound Assessment of Gastric Emptying of Korean Meals: Rice and Noodle
June 22, 2018 updated by: Jin-Young Hwang, SMG-SNU Boramae Medical Center
Ultrasound Assessment of Gastric Emptying of Korean Meals in Healthy Volunteer: Rice and Noodle
The investigators evaluate gastric emptying time of common Korean meals (rice, noodles) in healthy volunteers.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
The investigators assess the gastric volume and contents of healthy volunteers at 4, 5, 6, 7, 8 hours after eating common Korean meal (rice or noodle) using a ultrasonography.
Study Type
Observational
Enrollment (Anticipated)
60
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
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Adult healthy volunteers
Description
Inclusion Criteria:
- Adult healthy volunteers
Exclusion Criteria:
- History of gastrectomy
- Anatomical abnormalities or mass of 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 |
---|---|
Rice
Group that healthy volunteers eat rice.
|
The gastric volume and gastric content are assessed at 4, 5, 6, 7, and 8 hours after eating a meal.
|
Noodle
Group that healthy volunteers eat noodle.
|
The gastric volume and gastric content are assessed at 4, 5, 6, 7, and 8 hours after eating a meal.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Gastric emptying time
Time Frame: 1 hour
|
The time for digesting a meal
|
1 hour
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Incidence of full stomach
Time Frame: At 4, 5, 6, 7, and 8 hours after eating a meal.
|
The incidence of full stomach is assessed by using ultrasonography.
|
At 4, 5, 6, 7, and 8 hours after eating a meal.
|
Cross sectional area of the stomach
Time Frame: At 4, 5, 6, 7, and 8 hours after eating a meal.
|
The cross sectional area of the stomach is assessed by using ultrasonography in the supine and right lateral positions.
|
At 4, 5, 6, 7, and 8 hours after eating a meal.
|
Gastric volume
Time Frame: At 4, 5, 6, 7, and 8 hours after eating a meal.
|
The volume of stomach is assessed using the following formula; volume of stomach (mL) = 27.0 + 14.6 x cross-sectional area (right lateral position) - 1.28 x age.
|
At 4, 5, 6, 7, and 8 hours after eating a meal.
|
Type of gastric contents
Time Frame: At 4, 5, 6, 7, and 8 hours after eating a meal.
|
The type of gastric contents is assessed using ultrasonography.
|
At 4, 5, 6, 7, and 8 hours after eating a meal.
|
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 (Anticipated)
June 15, 2018
Primary Completion (Anticipated)
May 1, 2019
Study Completion (Anticipated)
May 1, 2019
Study Registration Dates
First Submitted
May 4, 2018
First Submitted That Met QC Criteria
June 22, 2018
First Posted (Actual)
June 26, 2018
Study Record Updates
Last Update Posted (Actual)
June 26, 2018
Last Update Submitted That Met QC Criteria
June 22, 2018
Last Verified
June 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- 20180504
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.
Clinical Trials on Preoperative Fasting
-
University Children's Hospital, ZurichCompleted
-
SMG-SNU Boramae Medical CenterNot yet recruitingPreoperative FastingKorea, Republic of
-
Tokat Gaziosmanpasa UniversityUnknownPreoperative FastingTurkey
-
Sheba Medical CenterWithdrawnDuration of Preoperative FastingIsrael
-
University Hospital, BrestCompletedPreoperative Fasting and HypotensionFrance
-
Academisch Medisch Centrum - Universiteit van Amsterdam...European Society of Anaesthesiology and Intensive CareRecruitingInsulin Resistance | Perioperative Care | Orthopedic Surgery | Intermittent Fasting | Carbohydrate Loading | Preoperative FastingNetherlands
-
Boston Intelligent Medical Research Center, Shenzhen...Tsinghua UniversityNot yet recruitingPreoperative Care
-
Cairo UniversityCompletedPreoperative SedationEgypt
-
Jiangsu HengRui Medicine Co., Ltd.Active, not recruitingPreoperative SedationChina
Clinical Trials on Evaluation of gastric volume and content
-
Hospices Civils de LyonCompletedPulmonary Aspiration of Gastric ContentsFrance
-
Centre Hospitalier Departemental VendeeUniversity Hospital, ToursCompletedVentilation-Associated PneumoniaFrance
-
Seoul National University HospitalUnknownGastroparesisKorea, Republic of
-
Istanbul UniversityCompletedNausea | Bleeding | Aspiration | Gastric VolumeTurkey
-
SMG-SNU Boramae Medical CenterNot yet recruitingStomach Filling
-
Seoul National University Bundang HospitalNot yet recruitingCerebral Palsy | Aspiration, Respiratory
-
Cairo UniversityUnknown
-
Central Hospital, Nancy, FranceUnknown
-
Washington University School of MedicineCompleted
-
University of CalgaryDepartment of Critical Care MedicineCompletedFluid Therapy | Cardiac Surgical ProceduresCanada