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NCT04860141 · ClinicalTrials.gov registry record · Phase 4

Efficacy of Preoperative Administration of Gabapentin in 3rd Molar Dental Extraction.

A Phase 4 study of Pain, Postoperative and Dental Pain and Sensation Disorder, sponsored by Loma Linda University.

Recruiting
Registry status
Phase 4
Development phase
98
Enrollment target
1
Study location

NCT04860141 is a Phase 4 study of Pain, Postoperative and Dental Pain and Sensation Disorder that is actively recruiting participants, run by Loma Linda University. The registered enrollment target is 98 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (64% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04860141, a Phase 4 study of Pain, Postoperative and Dental Pain and Sensation Disorder, is actively recruiting participants, sponsored by Loma Linda University.

RECRUITING
Registry status
Phase 4
Development phase
98 participants
Enrollment target
1
Study location

Study Summary

This study is a double-blind, randomized, prospective, placebo-controlled single-center clinical research study in which 600 mg of gabapentin or placebo will be administered 2 hours preoperatively to 49 patients each undergoing wisdom teeth extraction. We will measure intraoperative opioid use, severity of pain, the number of analgesics taken, and side effect profiles (e.g. nausea/vomiting, dizziness) at the following intervals, 4 hour, 8 hour, 12 hour, 24, and 72 hour post-procedure.

Interventions

  • DRUG Placebo
  • DRUG Gabapentin 600mg

Study Locations (1)

California

  • Loma Linda University Health - Loma Linda

Trial Details

FieldValue
Enrollment Target 98 participants
Start Date 2021-06-16
Est. Completion 2026-12
Phase Phase 4

Sponsor

Loma Linda University

237 total trials

What the Registry Record Tells You About NCT04860141

The ClinicalTrials.gov registry entry for NCT04860141 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 98 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (64% lower). The listed sponsor is Loma Linda University, which has 237 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT04860141 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT04860141 about?

NCT04860141 is a clinical study titled "Efficacy of Preoperative Administration of Gabapentin in 3rd Molar Dental Extraction.". This study is a double-blind, randomized, prospective, placebo-controlled single-center clinical research study in which 600 mg of gabapentin or placebo will be administered 2 hours preoperatively to 49 patients each undergoing wisdom teeth extraction. We will measure intraoperative opioid use, seve...

What is the current status of trial NCT04860141?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 98 participants. The study started on 2021-06-16. Estimated completion is 2026-12.

What conditions does trial NCT04860141 study?

This clinical trial studies the following conditions: Pain, Postoperative, Dental Pain and Sensation Disorder.

What interventions are being tested in trial NCT04860141?

The interventions under investigation include: Placebo (DRUG), Gabapentin 600mg (DRUG).

Who is sponsoring clinical trial NCT04860141?

This trial is sponsored by Loma Linda University, which has 237 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04860141 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.