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This Prospective Study Has 2 Objectives: First, to Assess the Post-obturation Pain Utilizing Bioceramic Sealer and One Cone Technique. Second, to Compare the Intensity of Post-obturation Pain Following Unintentional Sealer Extrusion

Sponsor
Abdulaziz Abdulmunim Alabdulmunim (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05621681
Collaborator
(none)
100
Enrollment
4
Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

Root canal treatment is essential step to eliminate pain and preserve tooth structures. However, errors could happen unintentionally such as ledge, perforation and sealer extrusion.

Pain through an endodontic treatment is one of the elements that most of the patients seek treatment to be relived.

One the current systemic review analyzed the pain after root canal treatment could be up to half the patients.

The purpose of this study is to evaluate and record the postoperative pain among patients who are undergoing root canal treatment.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    100 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Postoperative Pain Assessment Following Unintentional Bioceramic Sealer Extrusion
    Anticipated Study Start Date :
    Dec 1, 2022
    Anticipated Primary Completion Date :
    Feb 1, 2023
    Anticipated Study Completion Date :
    Apr 1, 2023

    Outcome Measures

    Primary Outcome Measures

    1. Each patient was given visual assessment scale to analyze the postoperative pain and assessing the change in different time intervals (6 hours,24 hours,2 days,3days and 4 days) [Five times intervals were recorded at the following: 6 hours following the treatment,1 day,2days,3days and 4 days]

      Visual analogue card scales contains numbers range from 0-10 1-3 indicates mild pain, while 4-6 suggests moderate pain and 7-10 specify sever pain.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Primary root canal Asymptomatic tooth with or without apical radiolucency Patient older than 18 and younger than 70 American Society of Anesthesiology (ASA) Class I or II
    Exclusion Criteria:
    • Patient with preoperative pain Periodontal probing more than 5mm When patency could not be achieved pregnant patient., patients who could not properly follow the instructions for filling the visual analog card (VAS) were excluded.

    Previously treated or initiated

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Abdulaziz Abdulmunim Alabdulmunim

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Abdulaziz Abdulmunim Alabdulmunim, Intern, Qassim University
    ClinicalTrials.gov Identifier:
    NCT05621681
    Other Study ID Numbers:
    • Abdulaziz Abdulmunim
    First Posted:
    Nov 18, 2022
    Last Update Posted:
    Nov 18, 2022
    Last Verified:
    Nov 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Abdulaziz Abdulmunim Alabdulmunim, Intern, Qassim University
    Sealer extrusion
    Postoperative pain
    Additional relevant MeSH terms:
    Pain, Postoperative

    Study Results

    No Results Posted as of Nov 18, 2022