Validation of a Dehydration Scoring System (VDSS)

This study has been completed.
Sponsor:
Information provided by:
Phoenix Children's Hospital
ClinicalTrials.gov Identifier:
NCT00931177
First received: July 1, 2009
Last updated: September 2, 2011
Last verified: September 2011
  Purpose

This is a study to evaluate the validity, reliability, and clinical usefulness of a new dehydration scoring system (DSS).


Condition Intervention
Dehydration
Other: weight
Other: weight and dehydration score

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Validation of a Dehydration Scoring System

Resource links provided by NLM:


Further study details as provided by Phoenix Children's Hospital:

Primary Outcome Measures:
  • Change in weight compared to dehydration score. [ Time Frame: 1 week ] [ Designated as safety issue: No ]

Enrollment: 102
Study Start Date: June 2009
Study Completion Date: November 2010
Primary Completion Date: June 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Dehydrated children
children with dehydration
Other: weight
weight and dehydration scores
Other: weight and dehydration score
weight and dehydration score
Other Name: weight and dehydration

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   1 Month to 15 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Dehydrated children

Criteria

Inclusion Criteria:

  • 1 mo - 15 yo children with DEHYDRATION from vomiting, diarrhea, or poor oral intake from presumed gastroenteritis
  • Previously healthy

Exclusion Criteria:

  • Preexisting cardiac, renal, or gastrointestinal disease
  • diabetes
  • failure to thrive
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00931177

Locations
United States, Arizona
Phoenix Children's Hospital
Phoenix, Arizona, United States, 85029
Sponsors and Collaborators
Phoenix Children's Hospital
Investigators
Principal Investigator: Mark Hostetler, MD Phoenix Children's Hospital
  More Information

Publications:
Responsible Party: Mark A Hostetler, MD, MPH - Principal Investigator, Phoenix Children's Hospital
ClinicalTrials.gov Identifier: NCT00931177     History of Changes
Other Study ID Numbers: VDSS
Study First Received: July 1, 2009
Last Updated: September 2, 2011
Health Authority: United States: Institutional Review Board

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

ClinicalTrials.gov processed this record on October 29, 2014