Skip to main content
OpenTrials
Completed

NCT Number: NCT00474721

Comparison of Acetaminophen With Codeine and Ibuprofen for Children With Injuries

We compared the pain relief of acetaminophen with codeine versus ibuprofen for children ages 5-18 years who came to the Pediatric Emergency Department with injuries to their arms or legs.

Completed

Looking for future studies?

Notify Me

Key information

Age range

5 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rady Children's Hospital

San Diego, California, 92123, United States

About this study

We conducted a randomized, double-blinded equivalence trial. Pediatric Emergency Department patients 5-18 years of age with acute extremity pain received acetaminophen-codeine (1 mg/kg as codeine) or ibuprofen (10 mg/kg). They provided Color Analog Scale pain scores at baseline and at 20, 40, and 60 minutes after medication administration. The primary outcome measured was the difference in changes in pain score at 40 minutes, compared against a previously described minimal clinically significant change in pain score of 2 cm. Additional outcomes included need for rescue medication and adverse effects.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 5 to 18 years of age
  • Spoke English as a primary language
  • Complained of an extremity injury with tenderness to palpation from the clavicle or femoral neck to the distal phalanges
  • Scored 5 or greater on a 10-point ordinal or Varni-Ryan pain scale administered at triage

Exclusion criteria

  • Allergy or prior adverse reaction to acetaminophen, codeine or ibuprofen;
  • Administration of any analgesic within 6 hours of presentation;
  • Significant deformity or vascular insufficiency of the extremity requiring immediate treatment as determined by the treating physician;
  • Inability to use the study pain instrument;
  • Any laceration near the suspected injury;
  • Chronic hepatic or renal disease;
  • Pregnancy in the third trimester;
  • Concurrent use of contraindicated medications such as monoamine oxidase inhibitors; or
  • Use of central nervous system depressants such as ethanol, benzodiazepines, barbiturates, antidepressants, or recreational drugs

Treatment and study plan

Ibuprofen

Drug

acetaminophen with codeine

Drug

Primary outcomes

  1. Change in color analog scale pain score

    Time frame: 40 minutes

Secondary outcomes

  1. adverse reaction

    Time frame: during ED stay

  2. need for rescue medication

    Time frame: during ED stay

  3. Change in pain score

    Time frame: 20 and 60 minutes

Sponsors and collaborators

Lead sponsor

University of California, San Diego

Other

Registry information

Official study title

A Randomized Blinded Comparison of Acetaminophen With Codeine and Ibuprofen for Treatment of Acute Pain in Children With Extremity Injuries

Important dates

Study start
2002
Study completion
2004
First posted
May 17, 2007
Registry last updated
May 17, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.