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Adhesive Cementation Materials and Techniques in Aesthetic Dentistry

R

Riga Stradins University

Status

Enrolling

Conditions

Dental Veneers
Orofacial Esthetic Scale
Resin Cements

Treatments

Procedure: Direct composite
Procedure: Porcelain veneers

Study type

Interventional

Funder types

Other

Identifiers

NCT07491809
6-DN-20/2/2026

Details and patient eligibility

About

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).

Enrollment

60 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • heavy bruxism, poor oral hygiene, active periodontal disease

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Porcelain veneers
Active Comparator group
Description:
Patients receiving porcelain veneers as an aesthetic treatment option
Treatment:
Procedure: Porcelain veneers
Direct composite restoration
Active Comparator group
Description:
Patients receiving direct composite injection moulding as an aesthetic treatment option
Treatment:
Procedure: Direct composite

Trial contacts and locations

1

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Central trial contact

Una Soboleva, Professor; Mara Gaile, DDS

Data sourced from clinicaltrials.gov

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