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Clinical Trials/NCT05621681
NCT05621681
Completed
Not Applicable

Postoperative Pain Assessment Following Unintentional Bioceramic Sealer Extrusion

Abdulaziz Abdulmunim Alabdulmunim1 site in 1 country145 target enrollmentJanuary 15, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Postoperative
Sponsor
Abdulaziz Abdulmunim Alabdulmunim
Enrollment
145
Locations
1
Primary Endpoint
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)
Status
Completed
Last Updated
2 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 15, 2023
End Date
July 15, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Abdulaziz Abdulmunim Alabdulmunim
Responsible Party
Sponsor Investigator
Principal Investigator

Abdulaziz Abdulmunim Alabdulmunim

Intern

Qassim University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

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)

Time Frame: 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.

Study Sites (1)

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