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NCT02635282 · ClinicalTrials.gov registry record · Phase 4

IN Ketamine Vs IN Midazolam and Fentanyl for Abscess I&D

A Phase 4 study, sponsored by University of Tennessee.

Completed
Registry status
Phase 4
Development phase
19
Enrollment target

NCT02635282: Completed Phase 4 study, sponsored by University of Tennessee.

NCT02635282 is a Phase 4 study that has completed, run by University of Tennessee. The registered enrollment target is 19 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02635282, a Phase 4 study, has completed, sponsored by University of Tennessee.

COMPLETED
Registry status
Phase 4
Development phase
19 participants
Enrollment target

Study Summary

The general objective of this study is to determine whether intranasal ketamine should be incorporated into formulary as an option to treat pain during minor procedures in the pediatric emergency department.

Primary Outcome

The Faces Pain Scale-Revised will be used for children ages 3-7 years

Interventions

  • DRUG intranasal ketamine
  • DRUG intranasal fentanyl
  • DRUG intranasal midazolam

Trial Details

FieldValue
Enrollment Target 19 participants
Start Date 2016-08
Est. Completion 2017-03-23
Phase Phase 4
University of Tennessee

96 total trials

What the finished NCT02635282 record still lists

NCT02635282 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 19 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 3 interventions - of which intranasal ketamine is the first listed.

NCT02635282 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02635282 about?

NCT02635282 is a clinical study titled "IN Ketamine Vs IN Midazolam and Fentanyl for Abscess I&D". The general objective of this study is to determine whether intranasal ketamine should be incorporated into formulary as an option to treat pain during minor procedures in the pediatric emergency department.

What is the current status of trial NCT02635282?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 19 participants. The study started on 2016-08. Estimated completion is 2017-03-23.

What interventions are being tested in trial NCT02635282?

The interventions under investigation include: intranasal ketamine (DRUG), intranasal fentanyl (DRUG), intranasal midazolam (DRUG).

Who is sponsoring clinical trial NCT02635282?

This trial is sponsored by University of Tennessee, which has 96 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02635282's enrollment target sits among peer trials

19 1834th of 2000 higher than 159 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 NCT02635282, the US trial registry maintained by the National Library of Medicine. NCT02635282 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.