- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02203123
Ratio of Inferior Vena Cava and Aorta Diameter in Dehydrated Children
July 28, 2014 updated by: Jin Hee Lee, Seoul National University Hospital
- There is no definite tool for measurement of dehydration in children
- Subjective clinical dehydration scale is considered as valuable scoring system, but it cannot be reliable among clinicians sometimes.
- Some authors found Inferior vena cava/Aorta ratio can be a objective marker for dehydration
- However, there is no evidence of correlation between clinical dehydration scale and inferior vena cava/aorta ratio
- We will observe correlation between clinical dehydration scale and inferior vena cava/aorta ratio and change of the ratio according to hydration with intravenous normal saline infusion.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
226
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Gyeonggi-do
-
Gumi-dong, Seongnam-si, Gyeonggi-do, Korea, Republic of, 463-707
- Recruiting
- Seoul National University Bundang Hospital
-
-
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
3 months to 15 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- All children with dehydration who visit emergency department
Exclusion Criteria:
- congenital heart disease
- bronchopulmonary dysplasia
- renal disease
- liver disease
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
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Ultrasound, inferior vena cava, aorta, normal saline
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
diameter of inferior vena cava and aorta
Time Frame: up to 2 hours
|
we will measure the diameter of inferior vena cava and aorta using ultrasound during every 10 ml/kg infusion of intravenous normal saline
|
up to 2 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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
March 1, 2014
Primary Completion (Anticipated)
April 1, 2015
Study Registration Dates
First Submitted
June 17, 2014
First Submitted That Met QC Criteria
July 28, 2014
First Posted (Estimate)
July 29, 2014
Study Record Updates
Last Update Posted (Estimate)
July 29, 2014
Last Update Submitted That Met QC Criteria
July 28, 2014
Last Verified
July 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ultrasound_01
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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