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NCT04500158 · ClinicalTrials.gov registry record · Phase 3

The Effect of Local Anesthesia on Control of Intraoperative Physiologic Parameters and Post Operative Comfort

A Phase 3 study, sponsored by Virginia Commonwealth University.

Completed
Registry status
Phase 3
Development phase
59
Enrollment target

NCT04500158: Completed Phase 3 study, sponsored by Virginia Commonwealth University.

NCT04500158 is a Phase 3 study that has completed, run by Virginia Commonwealth University. The registered enrollment target is 59 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04500158, a Phase 3 study, has completed, sponsored by Virginia Commonwealth University.

COMPLETED
Registry status
Phase 3
Development phase
59 participants
Enrollment target

Study Summary

The purpose of this study is to compare patient responses during and after surgery when local anesthetic is used for dental treatment under general anesthesia (GA) and when it is not used.

Primary Outcome

The Parent's Postoperative Pain Measure ( abbreviated: PPPM) Scale consists of 15 questions with scores ranging from 0 to 15, with one point assigned to each question answered with a "Yes" and therefore higher scores indicating worse postoperative pain. A score of 6 or greater is considered clinically significant pain which was tallied for the primary outcome measure (i..e number of participants experiencing clinically significant postoperative pain).

Interventions

  • DRUG Lidocaine

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2020-11-03
Est. Completion 2024-02-28
Phase Phase 3
Virginia Commonwealth University

558 total trials

What the finished NCT04500158 record still lists

NCT04500158 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 59 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (92% lower).

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

NCT04500158 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04500158 about?

NCT04500158 is a clinical study titled "The Effect of Local Anesthesia on Control of Intraoperative Physiologic Parameters and Post Operative Comfort". The purpose of this study is to compare patient responses during and after surgery when local anesthetic is used for dental treatment under general anesthesia (GA) and when it is not used.

What is the current status of trial NCT04500158?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 59 participants. The study started on 2020-11-03. Estimated completion is 2024-02-28.

What interventions are being tested in trial NCT04500158?

The interventions under investigation include: Lidocaine (DRUG).

Who is sponsoring clinical trial NCT04500158?

This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04500158's enrollment target sits among peer trials

59 1824th of 2000 higher than 176 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT04500158, the US trial registry maintained by the National Library of Medicine. NCT04500158 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.