The Effect of Clinical Experience on the Quality of Obturation and Periapical Changes of Teeth Treated With Matched Cones in Combination With Bioceramic Sealer
1 other identifier
interventional
54
1 country
1
Brief Summary
Evaluation of the impact of clinical experience on the quality of obturation and periapical changes of clinical cases using lateral compaction with bioceramic sealers and matched cone obturation with bioceramic sealers both clinically and radiographically.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2023
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2023
CompletedFirst Submitted
Initial submission to the registry
February 7, 2024
CompletedFirst Posted
Study publicly available on registry
February 15, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2025
CompletedFebruary 15, 2024
February 1, 2024
2.1 years
February 7, 2024
February 14, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Postoperative pain assessment
The postoperative pain assessment was done using the modified verbal descriptor scale as follows: None (Score0), Mild(Score1), Moderate (Score2), and severe (Score3).
24 hours
Postoperative pain assessment
The postoperative pain assessment was done using the modified verbal descriptor scale as follows: None (Score0), Mild(Score1), Moderate (Score2), and severe (Score3).
48 hours
Postoperative pain assessment
The postoperative pain assessment was done using the modified verbal descriptor scale as follows: None (Score0), Mild(Score1), Moderate (Score2), and severe (Score3).
72 hours
Postoperative pain assessment
The postoperative pain assessment was done using the modified verbal descriptor scale as follows: None (Score0), Mild(Score1), Moderate (Score2), and severe (Score3).
96 hours
Postoperative pain assessment
The postoperative pain assessment was done using the modified verbal descriptor scale as follows: None (Score0), Mild(Score1), Moderate (Score2), and severe (Score3).
120 hours
Secondary Outcomes (1)
The quality of obturation and the voids within the root canal filling
24 hours
Study Arms (4)
Experienced dentist using lateral compaction with bioceramic sealer group.
EXPERIMENTALThe canals in this group obturation were obturated by an Experienced dentist using lateral compaction with bioceramic sealer.
Unexperienced dentist using lateral compaction with bioceramic sealer group.
EXPERIMENTALThe canals in this group obturation were obturated by an Unexperienced dentist using lateral compaction with bioceramic sealer.
Experienced dentist using Single cone with bioceramic sealer group.
EXPERIMENTALThe canals in this group obturation were obturated by an Experienced dentist using Single cone with bioceramic sealer.
Unexperienced dentist using Single cone with bioceramic sealer group.
EXPERIMENTALThe canals in this group obturation were obturated by an Unexperienced dentist using Single cone with bioceramic sealer.
Interventions
Root canal treatment using bioceramic sealers.
Root canal treatment using bioceramic sealers.
Root canal treatment using bioceramic sealers.
Root canal treatment using bioceramic sealers.
Eligibility Criteria
You may qualify if:
- patients with symptoms of irreversible pulpitis without apical periodontitis related to the maxillary first premolar ranging from 20 to 40 years old and with separate roots were selected from patients referred to the diagnosis clinic, Faculty of dental medicine Al-Azhar University, Cairo, Boys branch.
You may not qualify if:
- Patients with any systemic disorders.
- Pregnancy.
- teeth with positive response to palpation test
- Non vital teeth.
- Teeth with positive response to percussion test.
- Teeth with mobility of grade II or III.
- teeth with probing depth more than 3 mm.
- Teeth with abnormal morphology.
- Teeth with root curvatures more than 20 degree (according to Schneider's method).
- Teeth with internal or external root resorption.
- Teeth with vertical root fracture.
- Teeth with open apices.
- Teeth with any root canal type other than type I.
- Patients with (VDS) test with score 4 or less. 15- teeth with fused roots or single root.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Al-Azhar university
Cairo, 11651, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant lecturer
Study Record Dates
First Submitted
February 7, 2024
First Posted
February 15, 2024
Study Start
January 1, 2023
Primary Completion
February 1, 2025
Study Completion
April 1, 2025
Last Updated
February 15, 2024
Record last verified: 2024-02