18-Month Clinical Evaluation of Self-Adhesive Flowable Giomer Compared to Conventional Flowable Giomer in Conservative Occlusal Restorations
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: FIT SA, Beautifil Flow Plus F00.
- Who it may be relevant to
- Registry conditions: Occlusal Caries. Basic parameters: from 18 years · 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
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
18-Month Clinical Evaluation of Self-Adhesive Flowable Giomer Compared to Conventional Flowable Giomer in Conservative Occlusal Restorations: A Randomized Clinical Trial
Overview
The study compares two restorative materials to restore occlusal decay, offering the patients high-strength, high-durability restorations with antibacterial properties.
Detailed description
There is no available evidence discussing the FIT SA restorative material in the restoration of occlusal lesions. This study aims to provide valuable insights into the clinical performance of this restorative material compared to the gold standard.
Interventions
- Other FIT SA
Self Adhesive Flowable giomer restorative material - Other Beautifil Flow Plus F00
Conventional Flowable giomer composite
Primary outcome measures
- Clinical performance [Time frame: 18 months]
Eligibility criteria
Inclusion criteria
- Posterior vital tooth with Class I caries.
Exclusion criteria
- Teeth with clinical symptoms of pulpitis, such as spontaneous pain.
- Pain or sensitivity to pressure.
- Non-vital teeth.
- Fractured or cracked teeth.
- Endodontically treated teeth.
- Periodontally affected teeth.
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
- Quadruple blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06956651 · 13579