- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01656863
Oral Rehydration Therapy in Children With Mild to Moderate Dehydration
August 2, 2012 updated by: Hillel Yaffe Medical Center
The purpose of this study is to determine parental attitudes towards oral rehydration therapy for children with mild to moderate dehydration.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
100
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
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-
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Hadera, Israel, 38100
- Hillel Yaffe Medical Center
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Parents of children suffering dehydration reporting to pediatric emergency room
Description
Inclusion Criteria:
- Parents of dehydrated children aged 0-18
Exclusion Criteria:
- Child with severe dehydration
- Child with chronic disease causing dehydration
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
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Parents
Parents reporting to the emergency room with dehydrated children
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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
August 1, 2012
Primary Completion (Anticipated)
August 1, 2013
Study Completion (Anticipated)
August 1, 2013
Study Registration Dates
First Submitted
August 1, 2012
First Submitted That Met QC Criteria
August 2, 2012
First Posted (Estimate)
August 3, 2012
Study Record Updates
Last Update Posted (Estimate)
August 3, 2012
Last Update Submitted That Met QC Criteria
August 2, 2012
Last Verified
August 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 00-15-12 HYMC
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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