Adhesive Cementation Materials and Techniques in Aesthetic Dentistry
1 other identifier
interventional
60
1 country
1
Brief Summary
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).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2025
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 30, 2025
CompletedFirst Submitted
Initial submission to the registry
March 16, 2026
CompletedFirst Posted
Study publicly available on registry
March 24, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2029
ExpectedMarch 24, 2026
March 1, 2026
8 months
March 16, 2026
March 19, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Patient satisfaction with porcelain veneers vs direct composite restorations using OES (orofacial aesthetic scale)
OES is a questionnaire with 8 questions regarding orofacial appearance. The higher the score, the more satisfied the patient is. 7 questions evaluate specific items, and number 8 is an overall assessment.
6 months, 1 year, 3 years
Secondary Outcomes (1)
Comparison of 2 veneer cements in terms of complications and discolouration
6 months, 1 year, 3 years
Other Outcomes (1)
Success and survival of porcelain veneers
6 months, 1 year, 3 years
Study Arms (2)
Porcelain veneers
ACTIVE COMPARATORPatients receiving porcelain veneers as an aesthetic treatment option
Direct composite restoration
ACTIVE COMPARATORPatients receiving direct composite injection moulding as an aesthetic treatment option
Interventions
Teeth preparation, laboratory made porcelain restoration cementation with 2 different cements
Digital modelling of teeth shapes, restoration with injectable composite directly
Eligibility Criteria
You may qualify if:
- healthy periodontium, needs at least 4 veneers, enamel around all veneer borders
You may not qualify if:
- heavy bruxism, poor oral hygiene, active periodontal disease
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Riga Stradins Universitylead
- Malmö Universitycollaborator
- Kuraray Noritake Dental Inc.collaborator
Study Sites (1)
Riga Stradins University
Riga, LV-1007, Latvia
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Christel Larsson, Professor
Malmo University
- STUDY DIRECTOR
Una Soboleva, Professor
Riga Stradins University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Researcher, D.D.S.
Study Record Dates
First Submitted
March 16, 2026
First Posted
March 24, 2026
Study Start
September 30, 2025
Primary Completion
June 1, 2026
Study Completion (Estimated)
August 1, 2029
Last Updated
March 24, 2026
Record last verified: 2026-03