Actively Recruiting
Evaluating the Clinical Success and Patient Satisfaction of Digital, Conventional, and Biomimetic Approaches for Restoring Endodontically Treated Teeth: Randomized Controlled Trial
Led by October University for Modern Sciences and Arts · Updated on 2024-12-16
42
Participants Needed
2
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating different approaches to restore endodontically treated mandibular first permanent molars, focusing on digital, conventional, and biomimetic techniques. The study aims to compare the clinical success, radiographic outcomes, and patient satisfaction of these methods in patients aged 15 years and older. Biomimetic dentistry uses advanced materials to mimic natural tooth function, potentially preserving more tooth structure and enhancing restoration durability. The trial compares three types of restorations: EverX Posterior with Vita Endo-Crowns, EverX Posterior with Bulk-Fill Resin Restorations, and Lithium Disilicate Endo-Crowns. These restorations use modern materials and CAD/CAM technology to simplify preparation and placement, often in a single visit. Biomimetic restorations focus on fiber-reinforced composites to strengthen bonding and evenly distribute chewing forces, aiming to reduce tooth stress and improve longevity. Participants will be reviewed over a 12-month period with clinical exams at 3, 6, 9, and 12 months. Researchers will assess restoration success using visual and tactile tools, radiographs to detect defects or infections, and patient questionnaires about satisfaction with shape, shade, chewing, and flossing ability. Data will be securely stored and analyzed to understand treatment outcomes, with safety and restoration durability monitored throughout the study.
CONDITIONS
Brief Title
Digital, Conventional, And Biomimetic Approaches for Restoring Endodontically Treated Teeth
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Endodontically-treated molar tooth with significant loss of tooth structure requiring cuspal coverage
- Patients aged 15 years or older
- Controlled dental disease with no active caries or periodontal disease
- Ability to be clinically reviewed for up to 1 year
You will not qualify if you...
- Poor oral hygiene
- Teeth with extensive cracks or fractures
- Deep subgingival margins greater than 0.5 mm
- Non-restorable teeth
- Non-functional teeth without opposing dentition
- Pocket probing depth greater than 3 mm
- Tooth mobility
- Patients with bruxism
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit
Duration - Single treatment visit
Participants receive one of the restorative treatments for their endodontically treated mandibular first permanent molar using digital, conventional, or biomimetic techniques.
1 treatment visit (in-person)
Duration - 12 months
Participants attend check-up visits to assess clinical success, radiographic outcomes, and patient satisfaction regarding their dental restoration.
Check-up visits at 3, 6, 9, and 12 months
Trial Site Locations
Total: 2 locations
1
MSA University
El-Sheikh Zayed City, Giza Governorate, Egypt, 16672
Actively Recruiting
2
MSA University
Giza, Egypt
Actively Recruiting
Research Team
M
Marwa Salmoon, Ph.D
M
Marwa A Salmoon, Ph.D
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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