Actively Recruiting

Phase Not Applicable
Age: 6Months - 36Months
All Genders
ID07074912

Prescription Antipyretics to Decrease Unscheduled Return Visits In A Pediatric Emergency Department

Led by University of Texas at Austin · Updated on 2025-07-20

440

Participants Needed

1

Research Sites

10 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating whether providing parents with a prescription for the correct weight-based doses of acetaminophen and ibuprofen reduces unscheduled return visits to the emergency department (ED) within one week for children evaluated for fever. This study focuses on children aged 6 to less than 36 months who are discharged from a pediatric ED. The goal is to understand if prescribing these common fever medicines affects return visits, patient satisfaction, and overall healthcare use. The study is a single-center, randomized controlled trial at a pediatric ED. Participants will be randomly assigned either to an intervention group that receives prescriptions for acetaminophen and ibuprofen with weight-based dosing or to a control group that receives standard printed discharge instructions including dosing information but no prescription. Both groups get the usual discharge education. The study involves 220 children in each group. After discharge, research staff will follow up by phone one week later to check if families made any unscheduled visits to the ED, urgent care, or clinics for similar complaints. They will also assess parental satisfaction with the care received. The main measure is whether an unscheduled return visit occurred within seven days. Secondary measures include total return visits, hospital admissions, and satisfaction levels. Caregivers will be informed about group assignment and asked for permission to continue using collected data for research.

CONDITIONS

Brief Title

Prescription Antipyretics to Decrease Unscheduled Return Visits In A Pediatric Emergency Department

Who Can Participate

Age: 6Months - 36Months
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children aged 6 to less than 36 months evaluated for fever and discharged home from Dell Children's Medical Center emergency department
  • Caregiver fluent in English or Spanish
Not Eligible

You will not qualify if you...

  • Previous enrollment in this study
  • Patient admitted to hospital
  • Parental request for a prescription for acetaminophen and/or ibuprofen
  • Trauma patient
  • Orthopedic complaint
  • Other painful indication for acetaminophen or ibuprofen
  • Acetaminophen or ibuprofen prescribed for anything other than fever
  • Allergy or contraindication to acetaminophen or ibuprofen
  • Parent and patient unlikely to follow up in the region (e.g., lives out of state)

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) during the emergency department visit

Treatment

Duration - Discharge day only

Participants are randomized to receive either a prescription with weight-based dosing for acetaminophen and ibuprofen or standardized printed discharge instructions without a prescription.

1 visit (in-person) at discharge from the emergency department

Follow-up

Duration - 7 days after discharge

Approximately one week after discharge, research personnel will contact participants to assess unscheduled return visits and parental satisfaction with emergency department care.

1 follow-up phone call

Trial Site Locations

Total: 1 location

1

Dell Children's Medical Center

Austin, Texas, United States, 78723

Actively Recruiting

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Research Team

L

Lina Palomares, RN, LMSW

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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