Prospective Comparative Study of the Efficacy of Common Antipyretic Treatments in Febrile Children
Primary Purpose
Fever
Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Ibuprofen
Acetaminophen
Sponsored by
About this trial
This is an interventional treatment trial for Fever focused on measuring acetaminophen, ibuprofen
Eligibility Criteria
Inclusion Criteria:
- fever between 38 and 41 Celsius (inclusive) on presentation to ER
- assessment by treating physician that patient requires antipyretic treatment
Exclusion Criteria:
- known allergy or hypersensitivity to either study medication
- received any antipyretic medication in past eight hours
- patient requires admission to hospital
- co-morbidities indicating increased risk of complication
- assessment by treating physician that patient is medically unsuitable for the study
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Experimental
Arm Label
acetaminophen
ibuprofen
combination
Arm Description
acetaminophen 15mg/kg (max 975mg)
ibuprofen 10mg/kg (max 600mg)
acetaminophen 15mg/kg (max 975mg) and ibuprofen 10mg/kg (max 600mg)
Outcomes
Primary Outcome Measures
temperature reduction from baseline
change in temperature from baseline at time of drug administration and at five minute intervals afterward for a minimum of one hour, maximum 4 hours
Secondary Outcome Measures
Full Information
NCT ID
NCT02294071
First Posted
November 17, 2014
Last Updated
November 17, 2014
Sponsor
Lawson Health Research Institute
1. Study Identification
Unique Protocol Identification Number
NCT02294071
Brief Title
Prospective Comparative Study of the Efficacy of Common Antipyretic Treatments in Febrile Children
Official Title
Prospective Comparative Study of the Efficacy of Common Antipyretic Treatments in Febrile Children
Study Type
Interventional
2. Study Status
Record Verification Date
November 2014
Overall Recruitment Status
Unknown status
Study Start Date
December 2014 (undefined)
Primary Completion Date
November 2015 (Anticipated)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Lawson Health Research Institute
4. Oversight
5. Study Description
Brief Summary
This study will examine in detail the immediate effects of three common treatments given to children with fevers to lower their temperature. Each child will be given either ibuprofen, acetaminophen, or a combination, and their temperature monitored at five-minute intervals. The temperature-lowering effects of each treatment will be compared to evaluate which is most effective.
Detailed Description
There is no substantial evidence that a fever lower than 41°C is harmful to the welfare of an otherwise healthy child, although they can be dangerous to children already in critical condition [1,2]. However, fevers in healthy children commonly cause anxiety in parents and caregivers, so parents and physicians often give antipyretic medications to lower the fever [3,4]. Ibuprofen and acetaminophen are two of the most commonly used medications in children. Most major pediatric medical associations agree about appropriate dosages for children, but give no clear guidelines on whether ibuprofen or acetaminophen should be used [3,5]. Physicians commonly make the decision between the two based on their personal opinions of the efficacy and safety of the medications, or based on habit [6]. Survey data shows that more than half of physicians use combinations of both acetaminophen and ibuprofen to treat fever, either simultaneously or on an alternating schedule, with a variety of dosing patterns [6]. A majority of physicians believed there were established guidelines supporting this use, but in fact there are not [6].
Combining the two medications is widely theorized to improve effectiveness, but clinical trials comparing combination treatments to ibuprofen and/or acetaminophen alone have shown inconsistent results [4,7-12]. Several pharmacodynamic studies have shown that ibuprofen and acetaminophen both produce their largest effects on temperature within the first hour following dosage [9,10,13-16]. Despite this, only one study has been performed examining the change in temperature at intervals shorter than 30 minutes, and that study used substandard monitoring methods [10].
This study will use gold-standard monitoring methods to take temperatures every five minutes through the first one to four hours of treatment. Understanding the pattern of temperature change in the acute stages after dosing will help settle the debate about the optimal medication choice for treating childrens' fevers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fever
Keywords
acetaminophen, ibuprofen
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
120 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
acetaminophen
Arm Type
Experimental
Arm Description
acetaminophen 15mg/kg (max 975mg)
Arm Title
ibuprofen
Arm Type
Experimental
Arm Description
ibuprofen 10mg/kg (max 600mg)
Arm Title
combination
Arm Type
Experimental
Arm Description
acetaminophen 15mg/kg (max 975mg) and ibuprofen 10mg/kg (max 600mg)
Intervention Type
Drug
Intervention Name(s)
Ibuprofen
Other Intervention Name(s)
Advil
Intervention Description
oral liquid ibuprofen 10mg/kg (maximum 600 mg)
Intervention Type
Drug
Intervention Name(s)
Acetaminophen
Other Intervention Name(s)
Tylenol
Intervention Description
oral liquid acetaminophen 15mg/kg (max 975mg)
Primary Outcome Measure Information:
Title
temperature reduction from baseline
Description
change in temperature from baseline at time of drug administration and at five minute intervals afterward for a minimum of one hour, maximum 4 hours
Time Frame
4 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
fever between 38 and 41 Celsius (inclusive) on presentation to ER
assessment by treating physician that patient requires antipyretic treatment
Exclusion Criteria:
known allergy or hypersensitivity to either study medication
received any antipyretic medication in past eight hours
patient requires admission to hospital
co-morbidities indicating increased risk of complication
assessment by treating physician that patient is medically unsuitable for the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michael J Rieder, MD
Phone
(519) 685-8500
Ext
58293
Email
mrieder@uwo.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Lauren Faught, PhD
Phone
519-661-3221
Email
lhanly2@uwo.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael J Rieder, MD
Organizational Affiliation
Western University, Canada
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
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21503807
Citation
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Prospective Comparative Study of the Efficacy of Common Antipyretic Treatments in Febrile Children
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