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The warm compress in the care of febrile children: Randomized Clinical Trial.

Not Applicable
Conditions
Fever
Child
Pediatric Nursing
Randomized Controlled Trial.
C23.888.119.344
M01.060.406
H02.478.676.631
V03.175.250.500.500
Registration Number
RBR-8h6qxv
Lead Sponsor
Escola de Enfermagem da Universidade de São Paulo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Data analysis completed
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Will be included in the study children from 1 month to 11 years 11 months and 29 days, who meet the following criteria:Present axillary temperature 37.8ºC; Interval between the administration of the antipyretic and the beginning of the treatment application, application of warm compresses, up to 10 minutes; Have permission from parents or guardians and agree to participate in the study.
In addition to these criteria, it will also be allowed to include the same patient within 12 hours of the last inclusion in the study and not be under the effect of antipyretic, it is necessary to have a minimum of 6 hours of the last antipyretic.

Exclusion Criteria

Patients with the diagnosis of malignant hyperthermia; neurological dysfunction; patients to undergo a procedure for up to 3 hours after administration of the antipyretic.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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