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NCT02595463 · ClinicalTrials.gov registry record · Phase 2

Intravenous Lidocaine for Post-Tonsillectomy Pain in Pediatric Patients

A Phase 2 study, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.

Completed
Registry status
Phase 2
Development phase
89
Enrollment target

NCT02595463 is a Phase 2 study that has completed, run by Ann & Robert H Lurie Children's Hospital of Chicago. The registered enrollment target is 89 participants.

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The verdict

NCT02595463, a Phase 2 study, has completed, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.

COMPLETED
Registry status
Phase 2
Development phase
89 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether giving lidocaine intravenously during and after a tonsillectomy surgery is effective in decreasing postoperative pain.

Interventions

  • DRUG Saline
  • DRUG Lidocaine

Trial Details

FieldValue
Enrollment Target 89 participants
Start Date 2015-11
Est. Completion 2024-07-05
Phase Phase 2

What the Registry Record Tells You About NCT02595463

The ClinicalTrials.gov registry entry for NCT02595463 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 89 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ann & Robert H Lurie Children's Hospital of Chicago, which has 159 total studies on file at ClinicalTrials.gov.

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

NCT02595463 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02595463 about?

NCT02595463 is a clinical study titled "Intravenous Lidocaine for Post-Tonsillectomy Pain in Pediatric Patients". The purpose of this study is to determine whether giving lidocaine intravenously during and after a tonsillectomy surgery is effective in decreasing postoperative pain.

What is the current status of trial NCT02595463?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 89 participants. The study started on 2015-11. Estimated completion is 2024-07-05.

What interventions are being tested in trial NCT02595463?

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

Who is sponsoring clinical trial NCT02595463?

This trial is sponsored by Ann & Robert H Lurie Children's Hospital of Chicago, which has 159 total clinical trials registered on ClinicalTrials.gov.

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

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.