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NCT04763876 · ClinicalTrials.gov registry record · Phase 4

Intramuscular Ketorolac at Two Single-Dose Regimens

A Phase 4 study, sponsored by William Beaumont Army Medical Center.

Completed
Registry status
Phase 4
Development phase
110
Enrollment target

NCT04763876: Completed Phase 4 study, sponsored by William Beaumont Army Medical Center.

NCT04763876 is a Phase 4 study that has completed, run by William Beaumont Army Medical Center. The registered enrollment target is 110 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (79% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04763876, a Phase 4 study, has completed, sponsored by William Beaumont Army Medical Center.

COMPLETED
Registry status
Phase 4
Development phase
110 participants
Enrollment target

Study Summary

The purpose of this study was to evaluate a single 15 mg intramuscular (IM) dose of ketorolac for analgesic non-inferiority versus a single 60 mg IM dose for the treatment of acute MSK pain in a military emergency department (ED) that services Department of Defense (DoD), Department of Veteran Affairs (VA), and foreign military beneficiaries

Primary Outcome

The mean difference of Visual Analog Scale scores between the two treatment groups measured at 60-minutes. The Visual Analog Scale used measures from 0 mm to 100mm. A higher score represents more degree of change. 13 mm was used as the non-inferiority margin. A difference between the two groups less than 13 mm demonstrates that 15 mg is non-inferior to 60 mg.

Interventions

  • DRUG Ketorolac Injection 15 mg
  • DRUG Ketorolac Injection 60 mg

Trial Details

FieldValue
Enrollment Target 110 participants
Start Date 2020-06-27
Est. Completion 2021-02-04
Phase Phase 4

What the finished NCT04763876 record still lists

NCT04763876 is an interventional study that assigns participants to a tested intervention. The registered 110 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 (79% lower).

The record links to 0 conditions, and to 2 interventions - of which Ketorolac Injection 15 mg is the first listed.

NCT04763876 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04763876 about?

NCT04763876 is a clinical study titled "Intramuscular Ketorolac at Two Single-Dose Regimens". The purpose of this study was to evaluate a single 15 mg intramuscular (IM) dose of ketorolac for analgesic non-inferiority versus a single 60 mg IM dose for the treatment of acute MSK pain in a military emergency department (ED) that services Department of Defense (DoD), Department of Veteran Affai...

What is the current status of trial NCT04763876?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 110 participants. The study started on 2020-06-27. Estimated completion is 2021-02-04.

What interventions are being tested in trial NCT04763876?

The interventions under investigation include: Ketorolac Injection 15 mg (DRUG), Ketorolac Injection 60 mg (DRUG).

Who is sponsoring clinical trial NCT04763876?

This trial is sponsored by William Beaumont Army Medical Center, which has 4 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04763876's enrollment target sits among peer trials

110 727th of 2000 higher than 1,264 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 NCT04763876, the US trial registry maintained by the National Library of Medicine. NCT04763876 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.