CompletedNot Applicable

Clinical Follow-up of Porcelain Veneering on Titanium Crowns Produced by Different Techniques

Turkey (Türkiye)27 participantsStarted 2018-10-10

Plain-language summary

This clinical study aimed to evaluate the short-term clinical performance of porcelain-veneered titanium crowns fabricated using two different techniques: conventional casting and CAD/CAM milling. Restorations were assessed according to FDI clinical evaluation criteria with respect to esthetic, functional, and biological outcomes during follow-up appointments.Clinical evaluations took place at baseline (2 days after luting) and following 3, 6, 12, and 18 months after luting.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients with good oral hygiene * no systemic conditions contraindicating restorative treatment, * either post-endodontic crown indication * structurally compromised teeth (e.g., fracture, wear, or discoloration) with healthy periodontal and endodontic status were included in the study. Exclusion Criteria: * Patients with gingival inflammation * furcation defects, * abnormal probing depths * abnormal attachment levels, * parafunctional habits were excluded from the study.

What they're measuring

Clinical performance of titanium-ceramic crowns evaluated using the Fédération Dentaire Internationale (FDI) World Dental Federation clinical criteria

Timeframe: Baseline, 3 months,6 months, 12 months, and 18 months

Trial details

NCT IDNCT07459842

SponsorEge University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-05-04

View on ClinicalTrials.gov More Titanium Ceramic Crown trials