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

Not Applicable

Active, not recruiting

• Conditions: Occlusal Caries
• Interventions: Procedure: VertiseTM flowable composite (Kerr,USA)

• Registration Number: NCT06260644
• Lead Sponsor: Cairo University

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.

Detailed Description

Not available

Study Timeline

• Status Verified: 2024-02
• Study Start: 2024-02-01
• Study First Submitted: 2024-02-07
• Study First Submitted QC: 2024-02-07
• Last Update Submitted: 2024-02-07
• Study First Posted: 2024-02-15
• Last Update Posted: 2024-02-15
• Primary Completion: 2025-09
• Study Completion: 2025-10

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 34

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.

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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.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Conventional flowable nano filled resin composite	VertiseTM flowable composite (Kerr,USA)	Repairing the old defective class I composite restoration by conventional nano filled flowable resin composite.
Self adhesive flowable resin composite	VertiseTM flowable composite (Kerr,USA)	Repairing the old defective class I composite restoration by self adhering flowable resin composite.

Primary Outcome Measures

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

Trial Locations

Locations (1)

Faculty of Dentistry; 🇪🇬 Cairo, Egypt