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NCT05074056 · ClinicalTrials.gov registry record · Phase 4

Ketorolac on Postoperative Pain Reduction in Pediatric Patients with Adenotonsillectomy

A Phase 4 study, sponsored by St. Louis University.

Completed
Registry status
Phase 4
Development phase
142
Enrollment target

NCT05074056: Completed Phase 4 study, sponsored by St. Louis University.

NCT05074056 is a Phase 4 study that has completed, run by St. Louis University. The registered enrollment target is 142 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (73% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05074056, a Phase 4 study, has completed, sponsored by St. Louis University.

COMPLETED
Registry status
Phase 4
Development phase
142 participants
Enrollment target

Study Summary

Postoperative pain management in the pediatric patient undergoing tonsillectomy is challenging. Despite being used in many procedures for postoperative pain management, perioperative ketorolac usage in pediatric tonsillectomy surgery is very limited. A recent survey showed that only 8.2% of anesthesiologists use NSAIDS for perioperative management of children with OSA undergoing adenotonsillectomy. The investigators propose to conduct a prospective, randomized study to investigate the opioid-sparing effect of perioperative ketorolac in pediatric patients who undergo tonsillectomies.

Primary Outcome

Change in pain score using the Wong-Baker FACES Pain Rating Scale (0-10 scale with 0 being "no hurt" and 10 being "hurts worst") and 0-10 Numeric Pain Intensity Scale (0-10 scale with 0 being "no pain" and 10 being "Worst pain").

Interventions

  • DRUG Ketorolac

Trial Details

FieldValue
Enrollment Target 142 participants
Start Date 2022-02-08
Est. Completion 2024-12-30
Phase Phase 4
St. Louis University

107 total trials

What the finished NCT05074056 record still lists

NCT05074056 is an interventional study that assigns participants to a tested intervention. The registered 142 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (73% lower).

The record links to 0 conditions, and to 1 intervention - of which Ketorolac is the first listed.

NCT05074056 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05074056 about?

NCT05074056 is a clinical study titled "Ketorolac on Postoperative Pain Reduction in Pediatric Patients with Adenotonsillectomy". Postoperative pain management in the pediatric patient undergoing tonsillectomy is challenging. Despite being used in many procedures for postoperative pain management, perioperative ketorolac usage in pediatric tonsillectomy surgery is very limited. A recent survey showed that only 8.2% of anesthes...

What is the current status of trial NCT05074056?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 142 participants. The study started on 2022-02-08. Estimated completion is 2024-12-30.

What interventions are being tested in trial NCT05074056?

The interventions under investigation include: Ketorolac (DRUG).

Who is sponsoring clinical trial NCT05074056?

This trial is sponsored by St. Louis University, which has 107 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05074056's enrollment target sits among peer trials

142 580th of 2000 higher than 1,421 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05074056, the US trial registry maintained by the National Library of Medicine. NCT05074056 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.