Status:

COMPLETED

Buffered vs. Unbuffered Local Anesthesia in Mandibular Molars Diagnosed With Symptomatic Irreversible Pulpitis

Lead Sponsor:

Indiana University

Conditions:

Symptomatic Irreversible Pulpitis

Eligibility:

All Genders

18-80 years

Phase:

PHASE4

Brief Summary

The purpose of this study is to determine whether one type of anesthetic (numbing medicine) will work better at numbing the nerve in a tooth than using a different type of anesthetic. A second purpose...

Detailed Description

40 subjects with a mandibular molar diagnosed with symptomatic irreversible pulpitis will be randomly allocated into 2 groups. One group will receive a total of 3 cartridges of a standard, unbuffered ...

Eligibility Criteria

Inclusion

  • Inclusion Criteria - In order to participate, subjects must:
  • Be between the ages of 18 and 80 years old
  • Have the ability and willingness to independently consent to treatment and study participation
  • Have an uncomplicated medical history (ASA I and II)
  • Not be pregnant
  • Have no allergies local anesthetics/sulfites (confirmed or self-reported)
  • Not be taking any medications that may affect the proper assessment of the anesthetic (no acetaminophen or short-acting NSAIDs such as ibuprofen within the previous 6 hours; no long-acting NSAIDs such as naproxen within the previous 16 hours)
  • Not require nitrous oxide during treatment, and the injection area should appear healthy with no other pre-existing conditions or infections that may compromise an accurate collection of data
  • Be experiencing signs of irreversible pulpitis (an exaggerated response to cold that lingers longer than 10 seconds) in a mandibular molar at the time of conducting the study
  • Exclusion Criteria - No subjects will have:
  • A negative response to cold in the proposed treatment tooth
  • A radiographic periradicular pathosis more advanced than a widened periodontal ligament or have an intraoral swelling

Exclusion

    Key Trial Info

    Start Date :

    February 14 2022

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    June 30 2022

    Estimated Enrollment :

    40 Patients enrolled

    Trial Details

    Trial ID

    NCT05227300

    Start Date

    February 14 2022

    End Date

    June 30 2022

    Last Update

    May 14 2024

    Active Locations (1)

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    Indiana University School of Dentistry Graduate Endodontics Dept.

    Indianapolis, Indiana, United States, 46202