Trials / Completed
CompletedNCT07434700
Clinical Performance of Lithium Disilicate Veneer-Fixed Dental Prostheses for Incisor Tooth Replacement
Lithium Disilicate Veneer-Fixed Dental Prostheses for Anterior Tooth Replacement: Clinical Case Series
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 23 (actual)
- Sponsor
- Damascus University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study evaluated a conservative treatment approach for replacing a missing upper front tooth (maxillary incisor). The treatment involved an all-ceramic, resin-bonded fixed dental prosthesis designed as a minimally invasive alternative to conventional bridges. The prostheses were fabricated from lithium disilicate glass-ceramic and were designed either with a single retainer (bonded to one adjacent tooth) or with two retainers (bonded to two adjacent teeth). All restorations were bonded using light-curing resin cement. The study assessed the clinical performance of these prostheses over a follow-up period of at least 12 months. Clinical evaluation included assessment of prosthesis integrity and function during the observation period.
Detailed description
This retrospective case series evaluated the short-term clinical performance of veneer fixed dental prostheses used to replace a missing maxillary incisor. The prostheses were fabricated from lithium disilicate glass-ceramic (IPS e.max Press). The retainers consisted of labial ceramic veneers bonded to the enamel surfaces of adjacent teeth. Two prosthetic designs were included: a single-retainer (cantilever) design and a two-retainer design. All veneer retainers were cemented using a light-curing resin cement according to standard adhesive clinical procedures. Existing patient records were reviewed to assess prosthesis survival and clinical success during follow-up visits. Survival was defined as the prosthesis remaining in situ during the observation period. Clinical success was evaluated based on prosthesis integrity, maintenance of function, and absence of technical complications such as fracture or loss of retention. Follow-up duration was at least 12 months after cementation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Lithium disilicate double retainer veneer bridge | Replacing missing maxillary incisor with single retainer lithium disilicate veneer bridge |
| DEVICE | Lithium disilicate single retainer veneer bridge | Replacing missing maxillary incisor with double retainer lithium disilicate veneer bridge |
Timeline
- Start date
- 2011-10-03
- Primary completion
- 2014-12-01
- Completion
- 2014-12-01
- First posted
- 2026-02-25
- Last updated
- 2026-02-25
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT07434700. Inclusion in this directory is not an endorsement.