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Clinical Trials in Egypt / NCT07005167
Starting soon Not applicable

Clinical Performance of Endocrowns Fabricated From Two Hybrid Ceramic Materials on Endodontically Treated Molars: A Randomized Clinical Trial

NCT07005167 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-06
Last updated
2025-06-05

Condition(s) studied

Endocrown Restoration

Investigational drug(s) / intervention(s)

endocrownsendocrowns

endocrowns: endocrowns made of HC hard blocks or cerasmart blocks to restore endo treated molars

endocrowns: endocrowns made of Cerasmart blocks to restore endo treated molars

Study summary

The goal of this study is to evaluate the clinical success rate (measured by retention) of endo-crowns fabricated from two hybrid ceramic materials (HC Hard blocks ) versus (Cerasmart) at 6, 12, and 18 months.

Secondary Objectives are:

1. To compare the incidence of restoration failures between the two materials
2. To assess marginal adaptation and marginal discoloration over time
3. To evaluate wear of opposing enamel quantitatively
4. To compare surface texture, color match, and luster between materials
5. To determine patient satisfaction with both types of restorations It will be a randomized, controlled, double-blind clinical trial with 1:1 allocation ratio.

Eligibility

Sex
ALL
Min age
21 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Age ≥21 years 2. Good general health (ASA I or II) 3. Willing and able to provide informed consent 4. Committed to follow-up appointments for 18 months 5. Root canal treated molars requiring restoration 6. Adequate remaining tooth structure: * Minimum 2mm ferrule height * Sufficient wall thickness (≥1.5mm) * At least 2 remaining walls 7. Opposing natural dentition or fixed prosthesis 8. Adequate periodontal health: * Probing depth ≤4mm * No bleeding on probing 9. Good oral hygiene with plaque score ≤20% 10. Sufficient mouth opening for clinical procedures 11. Normal occlusion and acceptable interocclusal space Exclusion Criteria: 1. Pregnant or lactating women 2. Severe bruxism or parafunctional habits 3. Active periodontal disease 4. Active caries or inadequate oral hygiene 5. Less than 2mm ferrule height after preparation 6. Apical pathology or inadequate root canal treatment 7. Tooth mobility grade II or III 8. Known allergy to materials used 9. Uncontrolled diabetes (HbA1c \>7.0%) 10. Radiation therapy in head and neck region 11. Temporomandibular joint disorders 12. History of poor compliance with dental appointments 13. Heavy smokers (\>10 cigarettes/day) 14. Chronic use of medications affecting salivary flow 15. Unable to understand study requirements 16. Evidence of pulpal or periapical pathology

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of Dentistry, Cairo University Cairo Egypt

More Cairo University trials in Egypt

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07005167 on ClinicalTrials.gov ↗ ← All trials in Egypt