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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05337358
Other study ID # CEBD-2021-3-040
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 1, 2021
Est. completion date April 11, 2023

Study information

Verified date April 2022
Source Cairo University
Contact Sameh Sh Abou-steit, PhD
Phone 01001891010
Email samehabousteit@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In patients with endodontically treated molar teeth indicated for endocrown, will the fiber reinforced FRC base and bonded CAD/CAM resin composite endocrowns restorations have a similar clinical performance to the conventional lithium disilicate endocrown over one year?


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date April 11, 2023
Est. primary completion date April 11, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: - Patients with good oral hygiene - Patients having one or more endodontically treated molars that need prosthetic restoration. - Molars should have enough tooth structure for endocrown restoration with minimum 3 walls with thickness not less than 1.5 mm and gingival step placed supragingival - Fully erupted molars - Molars free of developmental defect - Healthy periodontium - Absence of periapical pathosis - Acceptable endodontic treatment and proper bone support Exclusion Criteria: - Patients with bad oral hygiene - Patients with active periodontal disease - Patients with missing teeth opposing to the area intended for restoration - Patients with parafunctional habits or psychiatric problems or unrealistic expectation.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
endocrown
endocrown

Locations

Country Name City State
Egypt Cairo University Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary clinical performance Using the modified United States Public Health Service criteria (Modified USPHS)- categorical 2 years
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