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Clinical Trial Summary

Randomized (1:1 ratio) study of subcutaneous (SC) versus intravenous (IV) fluid rehydration in mildly to moderately dehydrated pediatric patients.


Clinical Trial Description

This is a prospective, randomized (1:1 ratio), open-label, parallel group, multicenter, multi-national, study of SC versus IV fluid rehydration in mildly to moderately dehydrated pediatric patients treated in the Emergency Department (ED), inpatient pediatric unit, and/or outpatient urgent care facility. It is expected that up to 186 patients, in order to achieve 148 evaluable patients, will be randomized in a 1:1 ratio to receive isotonic fluid rehydration by either SC administration with hylenex (150 Units) or IV without hylenex. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00773175
Study type Interventional
Source Halozyme Therapeutics
Contact
Status Completed
Phase Phase 4
Start date October 2008
Completion date December 2009

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