Skip to main content
Clinical Trials/NCT06260644
NCT06260644
Active, not recruiting
Not Applicable

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)

Cairo University1 site in 1 country34 target enrollmentFebruary 1, 2024
ConditionsOcclusal Caries

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Occlusal Caries
Sponsor
Cairo University
Enrollment
34
Locations
1
Primary Endpoint
Restoration clinical performance using FDI criteria
Status
Active, not recruiting
Last Updated
2 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
February 1, 2024
End Date
October 2025
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Soha Sayed Hosny

masters degree student

Cairo University

Eligibility Criteria

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\&
  • 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.

Outcomes

Primary Outcomes

Restoration clinical performance using FDI criteria

Time Frame: assessment will be done after the treatment then 6 months, 12 months and18 months.

FDI criteria mechanical parameters

Study Sites (1)

Loading locations...

Similar Trials