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Clinical Evaluation of Bioactive Injectable Resin Composite in Posterior Restorations

Clinical Evaluation of Bioactive Injectable Resin Composite Versus Conventional Nanohybrid Composite in Posterior Restorations, 18 m Randomized Controlled Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05499494
Enrollment
26
Registered
2022-08-12
Start date
2022-08-31
Completion date
2024-03-31
Last updated
2022-08-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Restoration Failure

Keywords

Injectable composite, Nano hybrid composite

Brief summary

The aim of the study is to evaluate the clinical performance of new bioactive injectable composite compared to nanohybrid composite during the restoration of posterior cavities

Detailed description

Statement of the problem: Marginal defects of composite fillings are often thought to be caused by poor adaptation of the restorative material to the cavity wall. To avoid these defects, particularly in posterior teeth, the use of flowable composites has been advocated because of their ability to 'wet' and adapt well to cavity margins and walls. However, flowable composites have a lower filler content and usually weaker mechanical properties than conventional composites. The continued development of resin composites has led to formulations designed to further simplify the filling procedure, provide better mechanical properties, reduce the effect of polymerization shrinkage stresses and improve aesthetics. Recently, a new type of highly filled flowable composite has been developed. It is characterized by its high viscosity and is claimed to have improved mechanical properties not dissimilar from conventional composite restorative materials. This composite contains nano-sized filler particles, and due to its consistency, the material has been referred to as an 'injectable composite'. Rationale for carrying out the trial: The rationale of this study is to evaluate the mechanical performance of injectable composite resin against nanohybrid composites, because of its easy handling, time-saving, better margin adaptation, and the gain of extra mechanical properties at the same time.

Interventions

OTHERBeautifil Flow Plus X F00 injectable composite

bioactive injectable composite

OTHERTetric N ceram resin composite

Nano hybrid resin composite

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Participants: 1. Age range 20-50 years. 2. Males Or females . 3. Co-operative patients approving to participate in the trial. * Teeth: 1. class I or II carious lesions premolars and molars. 2. Vital upper or lower teeth with no signs of irreversible pulpitis and pulpal necrosis. 3. Presence of favorable occlusion and teeth are in normal contact with the adjacent teeth.

Exclusion criteria

* Participants: 1. Patients with general systemic illness. 2. Allergic history against any component of used material. 3. Disabilities. 4. Pregnancy 5. Xerostomia. 6. Lack of compliance. 7. Evidence of parafunctional habits. 8. Temporomandibular joint disorders. * Teeth: 1. Periapical pathology or signs of pulpal pathology. 2. Endodontically treated teeth. 3. Tooth hypersensitivity. 4. Possible prosthodontic restoration of teeth. 5. Heavy occlusion and occlusal contacts or history of bruxism. 6. Severe periodontal affection.

Design outcomes

Primary

MeasureTime frameDescription
Change in the clinical performanceFrom baseline to 18 monthsMeasured using modified USPHS criteria

Countries

Egypt

Contacts

Primary ContactHazem Elderiny, M.SC
hazem.elderiny@dentistry.cu.edu.eg+201007775636
Backup ContactYomna Khallaf, PhD
Yomna.sayed@dentistry.cu.edu.eg+201006781076

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026