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NCT04642404 · ClinicalTrials.gov registry record · Phase 1

CBD for Dental Pain

A Phase 1 study of Toothache and Odontalgia, sponsored by The University of Texas Health Science Center at San Antonio.

Completed
Registry status
Phase 1
Development phase
64
Enrollment target
1
Study location

NCT04642404: Completed Phase 1 study of Toothache and Odontalgia, sponsored by The University of Texas Health Science Center at San Antonio.

NCT04642404 is a Phase 1 study of Toothache and Odontalgia that has completed, run by The University of Texas Health Science Center at San Antonio. The registered enrollment target is 64 participants, below the 143-participant average among 3 other Toothache trials with a reported enrollment target (55% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04642404, a Phase 1 study of Toothache and Odontalgia, has completed, sponsored by The University of Texas Health Science Center at San Antonio.

COMPLETED
Registry status
Phase 1
Development phase
64 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaulate CBD as a therapeutic approach for dental pain. Eligible subjects presented with emergency dental pain will be give a single dose of Epidiolex (FDA-approved CBD) or placebo and will be monitored for 3 hours for pain symptoms and psychologic effects.

Primary Outcome

Patients will report their pain level using a 100mm Visual Analogue Scale at baseline, measured at baseline and 180 minutes. Score is measured on a 100mm scale, scored 0-100, with a lower score indicating less pain.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Epidiolex 100 mg/mL Oral Solution

Study Locations (1)

Texas

  • The University of Texas Health Science Center at San Antonio - San Antonio

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2021-03-01
Est. Completion 2023-03-13
Phase Phase 1

What the finished NCT04642404 record still lists

NCT04642404 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, below the 143-participant average among 3 other Toothache trials with a reported enrollment target (55% lower).

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

NCT04642404 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT04642404 about?

NCT04642404 is a clinical study titled "CBD for Dental Pain". The purpose of this study is to evaulate CBD as a therapeutic approach for dental pain. Eligible subjects presented with emergency dental pain will be give a single dose of Epidiolex (FDA-approved CBD) or placebo and will be monitored for 3 hours for pain symptoms and psychologic effects.

What is the current status of trial NCT04642404?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 64 participants. The study started on 2021-03-01. Estimated completion is 2023-03-13.

What conditions does trial NCT04642404 study?

This clinical trial studies the following conditions: Toothache, Odontalgia.

What interventions are being tested in trial NCT04642404?

The interventions under investigation include: Placebo (DRUG), Epidiolex 100 mg/mL Oral Solution (DRUG).

Who is sponsoring clinical trial NCT04642404?

This trial is sponsored by The University of Texas Health Science Center at San Antonio, which has 378 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04642404 being conducted?

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

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Source: ClinicalTrials.gov NCT04642404, the US trial registry maintained by the National Library of Medicine. NCT04642404 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.