Clinical Assessment of CAD/CAM Fabricated Lithium-Disilicate Overlay Versus Lithium-disilicate Endocrowns for Restoration of Endodontically Treated Teeth.
1 other identifier
interventional
25
1 country
1
Brief Summary
A Randomized Controlled Clinical Study aims for Clinical Assessment of CAD/CAM Fabricated Lithium-Disilicate overlay in comparison to Lithium-disilicate Endocrowns for Restoration of Endodontically Treated Teeth.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Aug 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
March 15, 2024
CompletedFirst Submitted
Initial submission to the registry
March 9, 2026
CompletedFirst Posted
Study publicly available on registry
April 2, 2026
CompletedApril 2, 2026
March 1, 2026
7 months
March 9, 2026
March 31, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
marginal adaptations
Marginal adaptation will be evaluated using Modified United States Public Health Service (USPHS) criteria by two calibrated independent examiners. Scores will be recorded as Alpha, Bravo, or Charlie based on marginal integrity.
Baseline, 5 months, 10 months, 15 months, and 20 months
Secondary Outcomes (2)
marginal discoloration
Baseline, 5, 10, 15, and 20 months
patient satisfaction
20 months
Study Arms (2)
lithium disilicate endocrown
ACTIVE COMPARATORoverlay
ACTIVE COMPARATORInterventions
indirect partial coverage restoration that cover mainly the occlusal surface of posterior teeth
Eligibility Criteria
You may qualify if:
- Patients with endodontically treated teeth indicated to ceramic Endocrowns.
- Patients with endodontically treated teeth indicated to ceramic overlays.
- Physically and psychologically able to tolerate conventional restorative procedures.
- Have no active periodontal or periapical diseases.
- Maintenance of good oral hygiene.
- Willing to return for follow-up examinations and evaluation.
You may not qualify if:
- Patients in the growth stage with partially erupted teeth.
- Patients with para-functional habits.
- Patients with defective endodontic treatment.
- Patients with poor oral hygiene and motivation.
- Psychiatric problems or unrealistic expectations.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
- Ahram Canadian Universitycollaborator
Study Sites (1)
Faculty of Dentistry Cairo University
Cairo, Cairo Governorate, 12567, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- lecturer assisstant
Study Record Dates
First Submitted
March 9, 2026
First Posted
April 2, 2026
Study Start
August 1, 2023
Primary Completion
March 1, 2024
Study Completion
March 15, 2024
Last Updated
April 2, 2026
Record last verified: 2026-03