Evaluation of Using Self-adhering Flowable Resin Composite in Repairing Old Defective Resin Composite Restorations Over 18 Months Follow up. (A Randomized Clinical Trial)

Evaluation of Using Self-adhering Flowable Resin Composite Versus Conventional Nano-filled Flowable Resin Composite in Repairing Old Defective Resin Composite Restorations Over 18 Months Follow up. (A Randomized Clinical Trial)

Status

Active, not recruiting

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06260644

Enrollment

Registered

2024-02-15

Start date

2024-02-01

Completion date

2025-10-31

Last updated

2024-02-15

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

Conditions

Occlusal Caries

Keywords

flowable resin composite

Brief summary

This research proposal is evaluating the clinical performance of using self-adhering flowable resin composite in repairing old occlusal defective resin composite versus conventional flowable resin composite restoration over 18 months.

Interventions

PROCEDUREVertiseTM flowable composite (Kerr,USA)

self adhesive flowable resin composite restoration.

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

DOUBLE (Subject, Outcomes Assessor)

Masking description

double ( participants, outcomes assessor) participants and both assessors will be blind to the type of material used

Intervention model description

parallel assignment

Eligibility

Sex/Gender

ALL

Age

18 Years to 35 Years

Healthy volunteers

Inclusion criteria

* Patients (18-35 y) * patients with defective resin composite class I restorations that need repair. * dental motivated patients who attends regularly. * Vital posterior teeth with repairable defective resin composite class I restorations. * Localized marginal defect or marginal staining FDI 3& 4. * Teeth with no or minimum mobility & healthy peridontium. * No history of any irreversible pulpal pain or necrosis in the teeth to be restored.

Exclusion criteria

* • Patients with defective restorations that dictate replacement * Uncooperative behavior limits the isolation techniques throughout the procedure. * Presence of parafunctional habits. * Patient with history of systemic medical disease, or any other serious relevant problem. * High caries risk patients. Periodontal disease that may affect the prognosis of the restoration or the tooth itself. * Fractured or visibly cracked teeth. * Symptoms of any pulp pathosis. * Defective resin composite restorations that dictate replacement.

Design outcomes

Primary

Measure	Time frame	Description
Restoration clinical performance using FDI criteria	assessment will be done after the treatment then 6 months, 12 months and18 months.	FDI criteria mechanical parameters

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026