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

RECRUITING Phase 4

Comparing Analgesic Regimen Effectiveness and Safety for Surgery for Kids Trial

NCT06671002 · View on ClinicalTrials.gov ↗

Study Summary

This trial is being completed to compare two commonly used options to treat pain after discharge from surgery. Participants that undergo tonsil removal, gallbladder removal, and knee scope will be eligible to enroll. Eligible participants will be randomized to prescription of 1 of 2 groups of medications (Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) plus acetaminophen or low dose opioids with the NSAIDs plus acetaminophen. The key question the study seeks to answer is which option will have the best outcomes and with the fewest side effects?

Interventions

  • DRUG Acetaminophen
  • DRUG Ibuprofen
  • DRUG NSAID
  • DRUG Opioid

Study Locations (4)

California

  • Children's Hospital Los Angeles (CHLA) — Los Angeles
  • Lucile Packard Children's Hospital Stanford — Palo Alto

Michigan

  • University of Michigan — Ann Arbor

Ohio

  • Nationwide Children's (NCH) — Columbus

Trial Details

FieldValue
Enrollment Target 900 participants
Start Date 2025-01-10
Est. Completion 2027-10-31
Phase Phase 4

Sponsor

University of Michigan

1,126 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06671002

The ClinicalTrials.gov registry entry for NCT06671002 describes a study currently listed as recruiting. It is categorized as Phase 4, 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 900 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Michigan, which has 1,126 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Surgery appearing as the primary indexed condition, and to 4 interventions — of which Acetaminophen 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: NCT06671002 reports 4 study locations spanning 3 distinct geographic areas — top geographies include California, Michigan, Ohio. 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 NCT06671002 about?

NCT06671002 is a clinical study titled "Comparing Analgesic Regimen Effectiveness and Safety for Surgery for Kids Trial". This trial is being completed to compare two commonly used options to treat pain after discharge from surgery. Participants that undergo tonsil removal, gallbladder removal, and knee scope will be eligible to enroll. Eligible participants will be randomized to prescription of 1 of 2 groups of medica...

What is the current status of trial NCT06671002?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 900 participants. The study started on 2025-01-10. Estimated completion is 2027-10-31.

What conditions does trial NCT06671002 study?

This clinical trial studies the following conditions: Surgery, Pain, Post Operative. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06671002?

The interventions under investigation include: Acetaminophen (DRUG), Ibuprofen (DRUG), NSAID (DRUG), Opioid (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06671002?

This trial is sponsored by University of Michigan, which has 1,126 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06671002 being conducted?

This trial has 4 study locations across California, Michigan, Ohio. 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