Status:
COMPLETED
Pediatric Fast Fluid Randomized Controlled Trial
Lead Sponsor:
McMaster Children's Hospital
Conditions:
Fluid Resuscitation
Eligibility:
All Genders
Phase:
NA
Brief Summary
The purpose of this study is to determine the impact of syringe size on the amount of time it takes a health care provider to administer a known volume (900 mL) of resuscitation fluid to a non-clinica...
Detailed Description
The Surviving Sepsis Guideline for the resuscitation of pediatric septic shock indicates that up to 60 mL/kg of isotonic saline should be administered within the first 15 minutes of resuscitation. The...
Eligibility Criteria
Inclusion
- Consenting health care staff and health care students capable of performing manual syringe bolus fluid administration
Exclusion
- Non-English speaking individuals
- Any condition that would impact upon the individual's ability to perform manual fluid resuscitation e.g. limited hand strength or dexterity
Key Trial Info
Start Date :
October 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2012
Estimated Enrollment :
48 Patients enrolled
Trial Details
Trial ID
NCT01494116
Start Date
October 1 2011
End Date
January 1 2012
Last Update
February 28 2012
Active Locations (1)
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1
Hamilton Health Sciences, McMaster Children's Hospital
Hamilton, Ontario, Canada, L8N3Z5