Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06505148

Comparing the Difference in Pain Control in the Pediatric General Surgery Population: to Alternate or Combine Acetaminophen and Ibuprofen?

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Baylor Research Institute · Academic / Other
Sex
All
Age
3 Years – 18 Years
Healthy volunteers
Not accepted

Summary

To examine the difference in pain control in the pediatric general surgery population alternating acetaminophen and Ibuprofen q 3 hours vs giving them simultaneous combination therapy around the clock.

Detailed description

The purpose of the study is to compare the difference in pain control in the pediatric general surgery population of those who receive alternating acetaminophen and ibuprofen every 3 hours to those who receive acetaminophen and ibuprofen combined therapy around the clock. Additionally, to investigate the difference in parent adherence to pain treatment plans between the alternating group from the combined group.

Conditions

Interventions

TypeNameDescription
DRUGAcetaminophenadministered alternatively with other drug
DRUGIbuprofenadministered alternatively with other drug

Timeline

Start date
2024-08-01
Primary completion
2025-08-01
Completion
2025-08-01
First posted
2024-07-17
Last updated
2024-07-22

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06505148. Inclusion in this directory is not an endorsement.