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
NCT ID: NCT05621681
Last Updated: 2024-04-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
145 participants
OBSERVATIONAL
2023-01-15
2023-07-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Incidence of Postoperative Pain After Using Different Types of Sealers
NCT05841290
The Effect of Different Obturation Techniques on Postobturation Pain in Single-Visit Root Canal Treatment
NCT06146894
Post-endodontic Pain Survey
NCT04462731
Postoperative Pain Evaluation After Obturation With Different Sealers
NCT07018284
Effect of Resin, Calcium Silicate and Silicone Based Root Canal Sealers on Postoperative Pain
NCT05033093
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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
18 Years
70 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Abdulaziz Abdulmunim Alabdulmunim
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Abdulaziz Abdulmunim Alabdulmunim
Intern
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Abdulaziz Abdulmunim
Buraidah, Al-Qassim Region, Saudi Arabia
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Abdulaziz Abdulmunim
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.