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

Occlusal Caries Clinical Trial

Official title:

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)

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT06260644
• Other study ID #: Repairing defective composite
• Status: Active, not recruiting
• Phase: N/A
• Start date: February 1, 2024
• Est. completion date: October 2025

Study information

• Verified date: February 2024
• Source: Cairo University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 34
• Est. completion date: October 2025
• Est. primary completion date: September 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 35 Years

Eligibility

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.

Related Conditions & MeSH terms

• Occlusal Caries

Intervention

Procedure:
• VertiseTM flowable composite (Kerr,USA)
self adhesive flowable resin composite restoration.

Locations

Country	Name	City	State
Egypt	Faculty of Dentistry	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

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