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Oral Rehydration Therapy in Children With Mild to Moderate Dehydration

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ClinicalTrials.gov Identifier: NCT01656863
Recruitment Status : Unknown
Verified August 2012 by Hillel Yaffe Medical Center.
Recruitment status was:  Not yet recruiting
First Posted : August 3, 2012
Last Update Posted : August 3, 2012
Sponsor:
Information provided by (Responsible Party):
Hillel Yaffe Medical Center

Study Description
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information
Brief Summary:
The purpose of this study is to determine parental attitudes towards oral rehydration therapy for children with mild to moderate dehydration.

Condition or disease Intervention/treatment
Parent Attitudes Other: Questionnaire

Study Design
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Study Type : Observational
Estimated Enrollment : 100 participants
Observational Model: Case-Only
Time Perspective: Prospective
Study Start Date : August 2012
Estimated Primary Completion Date : August 2013
Estimated Study Completion Date : August 2013

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Dehydration
U.S. FDA Resources

Groups and Cohorts
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Group/Cohort Intervention/treatment
Parents
Parents reporting to the emergency room with dehydrated children
 Other: Questionnaire


Outcome Measures
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Eligibility Criteria
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Parents of children suffering dehydration reporting to pediatric emergency room
Criteria

Inclusion Criteria:

  • Parents of dehydrated children aged 0-18

Exclusion Criteria:

  • Child with severe dehydration
  • Child with chronic disease causing dehydration
Contacts and Locations
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01656863


Contacts
Contact: Vered Nir, MD 972-4-630-4331 verednr@yahoo.com

Locations
Israel
Hillel Yaffe Medical Center
Hadera, Israel, 38100
Sponsors and Collaborators
Hillel Yaffe Medical Center
More Information
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Responsible Party: Hillel Yaffe Medical Center
ClinicalTrials.gov Identifier: NCT01656863     History of Changes
Other Study ID Numbers: 00-15-12 HYMC
First Posted: August 3, 2012    Key Record Dates
Last Update Posted: August 3, 2012
Last Verified: August 2012

Keywords provided by Hillel Yaffe Medical Center:
Dehydration

Additional relevant MeSH terms:
Dehydration
Water-Electrolyte Imbalance
Metabolic Diseases
Pathologic Processes