Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

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

NCT07074912 · View on ClinicalTrials.gov ↗

Study Summary

The study aims to evaluate whether unscheduled return visits within one week for similar complaints are impacted by ensuring parents leave the emergency department (ED) with a prescription for appropriately dosed acetaminophen and ibuprofen for their child.

Conditions Studied

Interventions

  • OTHER Prescription for weight-based dosing of antipyretic
  • OTHER Standard discharge instructions

Study Locations (1)

Texas

  • Dell Children's Medical Center — Austin

Trial Details

FieldValue
Enrollment Target 440 participants
Start Date 2024-12-15
Est. Completion 2026-03-15
Phase NA

Sponsor

University of Texas at Austin

225 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07074912

The ClinicalTrials.gov registry entry for NCT07074912 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 440 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Texas at Austin, which has 225 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Fever appearing as the primary indexed condition, and to 2 interventions — of which Prescription for weight-based dosing of antipyretic is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07074912 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07074912 about?

NCT07074912 is a clinical study titled "Prescription Antipyretics to Decrease Unscheduled Return Visits In A Pediatric Emergency Department". The study aims to evaluate whether unscheduled return visits within one week for similar complaints are impacted by ensuring parents leave the emergency department (ED) with a prescription for appropriately dosed acetaminophen and ibuprofen for their child.

What is the current status of trial NCT07074912?

This trial is currently recruiting. It is a NA study. The enrollment target is 440 participants. The study started on 2024-12-15. Estimated completion is 2026-03-15.

What conditions does trial NCT07074912 study?

This clinical trial studies the following conditions: Fever. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07074912?

The interventions under investigation include: Prescription for weight-based dosing of antipyretic (OTHER), Standard discharge instructions (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07074912?

This trial is sponsored by University of Texas at Austin, which has 225 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07074912 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial