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

Postoperative Pain Assessment Following Unintentional Bioceramic Sealer Extrusion

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05621681

Enrollment

145

Registered

2022-11-18

Start date

2023-01-15

Completion date

2023-07-15

Last updated

2024-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endodontic Overfill, Pain, Postoperative

Keywords

Sealer extrusion, Postoperative pain

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.

Interventions

None listed

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 70 Years

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

Design outcomes

Primary

Measure	Time frame	Description
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.

Countries

Saudi Arabia

Outcome results