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NCT02229578 · ClinicalTrials.gov registry record · Phase 4

Lidocaine For Treatment of Post-operative Pain From Donor Sites Following Burn Injury.

A Phase 4 study, sponsored by University of Florida.

Completed
Registry status
Phase 4
Development phase
34
Enrollment target

NCT02229578 is a Phase 4 study that has completed, run by University of Florida. The registered enrollment target is 34 participants.

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The verdict

NCT02229578, a Phase 4 study, has completed, sponsored by University of Florida.

COMPLETED
Registry status
Phase 4
Development phase
34 participants
Enrollment target

Study Summary

Burn pain is known to be one the most severe forms of acute pain often requiring large amounts of narcotics in addition to other adjuvants. Topical lidocaine is effective for controlling pain in various settings including dressing changes of burns. The aim of this study is to demonstrate the effectiveness of topical lidocaine in decreasing pain scores and narcotic requirements when applied to donor graft sites while at the same time not interfering with the standard of care TheraBond dressing. During this study the investiagtors will be monitoring for evidence of delayed wound healing, and surgical site infection.

Interventions

  • DRUG Placebo
  • DRUG Lidocaine

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2014-09
Est. Completion 2017-11-14
Phase Phase 4

Sponsor

University of Florida

1,106 total trials

What the Registry Record Tells You About NCT02229578

The ClinicalTrials.gov registry entry for NCT02229578 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 34 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Florida, which has 1,106 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02229578 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02229578 about?

NCT02229578 is a clinical study titled "Lidocaine For Treatment of Post-operative Pain From Donor Sites Following Burn Injury.". Burn pain is known to be one the most severe forms of acute pain often requiring large amounts of narcotics in addition to other adjuvants. Topical lidocaine is effective for controlling pain in various settings including dressing changes of burns. The aim of this study is to demonstrate the effecti...

What is the current status of trial NCT02229578?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 34 participants. The study started on 2014-09. Estimated completion is 2017-11-14.

What interventions are being tested in trial NCT02229578?

The interventions under investigation include: Placebo (DRUG), Lidocaine (DRUG).

Who is sponsoring clinical trial NCT02229578?

This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.