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)
Verified date | February 2024 |
Source | Cairo University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
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. |
Country | Name | City | State |
---|---|---|---|
Egypt | Faculty of Dentistry | Cairo |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
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. |
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT04463342 -
Evaluation of Clinical Performance for Recent Non Coated Glass Ionomer in Posterior Teeth
|
Phase 1 | |
Not yet recruiting |
NCT04532671 -
Evaluation of Clinical Performance of 3D Printed Polyether Ether Ketone (PEEK) Inlays
|
N/A | |
Not yet recruiting |
NCT06097143 -
Clinical Performance of Flowable Giomer Versus Nanofilled Composite in Conservative Occlusal Cavities
|
N/A | |
Not yet recruiting |
NCT04354636 -
Management of Occlusal Caries Using Silver Modified Atraumatic Restorative Treatment Versus Atraumatic Restorative Treatment
|
Phase 2/Phase 3 | |
Recruiting |
NCT05969756 -
Early Treatments for Preventing Occlusal Caries Lesions
|
N/A |