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Alternating acetaminophen and ibuprofen in the treatment of children with acute fever: a randomized controlled trial.

Alternating acetaminophen and ibuprofen in the treatment of children with acute fever: a randomized controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003440
Enrollment
Unknown
Registered
2013-04-30
Start date
2013-06-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute fever in children

Interventions

A group (experimental group):alternating acetaminophen and ibuprofen
B group (control group 1):acetaminophen monotherapy
C group (control group 2):ibuprofen monotherapy

Sponsors

Department of Paediatrics, West China Second University Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 5 Years

Inclusion criteria

Inclusion criteria: Febrile children aged 6 months to 5 years will be eligible if their anxillary temperature are equal to or greater than 38.5? and their history of fever are less than 3 days.

Exclusion criteria

Exclusion criteria: Children will be excluded if they have any of the following conditions: mild or more severer dehydration, known allergy or contraindication to any antipyretic, any acute or chronic hepatic disease, all acute or chronic renal disease with the exception of urinary tract infection, known coagulation abnormalities or active bleeding disorders, blood system diseases, malignancy, digestive ulcer, asthma or bronchiolitis, chronic metabolic disease, immune system diseases and require hormone therapy, any neurological or skin disease that may affect central thermoregulation, hypertension, critical ill condition, any medical or surgical condition that preclude take or absorb antipyretic (such as frequent vomiting), a history of any antipyretic or medicine with antipyretic effect use in the preceding 8 hours, require to take medicine which affect temperature (such as Topiramate). Children will also be excluded if they have taken part in this trial one time.

Design outcomes

Primary

MeasureTime frame
Non-communicating Children’s Pain Checklist – Revised (NCCPC-R) score;axillary temperature;

Secondary

MeasureTime frame
incidence of persistent fever;incidence of poor antipyretic effect;times of antipyretic use;incidence of low body temperature;incidence of rash for all causes;incidence of asthma for all causes;incidence of gastrointestinal symptoms for all cause ;incidence of hepatic dysfunction for all causes;incidence of renal dysfunction for all cause;

Countries

China

Contacts

Public ContactWan Chaomin
wcm0220@sina.com+86 13980915296

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 8, 2026