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Recruiting NCT07491809

Adhesive Cementation Materials and Techniques in Aesthetic Dentistry

No phase Interventional Dental Veneers Resin Cements Composite Restoration Orofacial Esthetic Scale

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Porcelain veneers, Direct composite.
Who it may be relevant to
Registry conditions: Dental Veneers, Resin Cements, Composite Restoration, Orofacial Esthetic Scale. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Latvia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Adhesive Cementation Materials and Techniques in Aesthetic Dentistry and Their Effect on the Longevity of Porcelain Veneers

Overview

AIM: To determine the most effective cementation method and resin cement material for long term success of esthetical restorations TASKS: 1. Compare Panavia Veneer LC (Kuraray Noritake) cement with universal Panavia V5 (Kuraray Noritake) cement for porcelain veneer cementation in terms of marginal defects and discolouration; 2. Evaluating direct vs indirect restorations after 1-year and 3-year follow up periods in terms of patient satisfaction (evaluated by OES scale). MATERIAL AND METHODS: Participants: Patients attending the Department of Prosthodontics at the RSU Institute of Stomatology, and willing to improve the aesthetics of front teeth with porcelain veneers. Approx. 30 patients. Inclusion criteria: healthy periodontium, needs 4 veneers, stable occlusion. Exclusion criteria: heavy bruxism, poor oral hygiene, active periodontal inflammation. Veneer preparations will be done for maxillary anterior teeth approximately 0.5mm deep, involving the whole facial surface and keeping enamel around all borders. For digital impressions of preparations intra-oral scans with intraoral scanner (3Shape TRIOS 5 WIRELESS, Denmark) will be taken. Veneers will be fabricated according to the CAD/CAM technique. This will be a prospective paired design study, i.e., two different composite cements (Panavia V5 and Panavia Veneer LC) will be used for each patient, cementing two veneers with each of the cements. Data on following variables will be collected: 1. Restoration condition (defects related to restoration - ceramic fractures, cracks, loss of retention, discolouration); 2. Condition of the abutment teeth (secondary caries, endodontic complications); 3. Periodontal condition (probing depth, bleeding on probing, gum recessions); 4. Patient satisfaction questionnaire (OES).

Interventions

  • Procedure Porcelain veneers
    Teeth preparation, laboratory made porcelain restoration cementation with 2 different cements
  • Procedure Direct composite
    Digital modelling of teeth shapes, restoration with injectable composite directly

Primary outcome measures

  • Patient satisfaction with porcelain veneers vs direct composite restorations using OES (orofacial aesthetic scale) [Time frame: 6 months, 1 year, 3 years]
Secondary outcome measures (1)
  • Comparison of 2 veneer cements in terms of complications and discolouration [Time frame: 6 months, 1 year, 3 years]

Eligibility criteria

Inclusion criteria

  • healthy periodontium, needs at least 4 veneers, enamel around all veneer borders

Exclusion criteria

  • heavy bruxism, poor oral hygiene, active periodontal disease

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Latvia · 1 center
  • Riga Stradins University — Riga

Identifiers

NCT: NCT07491809 · 6-DN-20/2/2026

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗