Trials / Completed
CompletedNCT04266210
Clinical Evaluation of a Restorative Glass Ionomer and a Composite Resin for the Restoration
Clinical Evaluation Two Restorative Systems in Non-carious Cervical Lesions at Patients With Different Systemic Diseases
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- Hacettepe University · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The clinical performances of a restorative glass ionomer and a composite resin will be compared in the restoration of non-carious cervical lesions (NCCLs) at patients with systemic diseases. After recruiting participants with at least 2 NCCLs and at least one systemic disease, all restorations will be placed by a single clinician. All lesions will be cleaned before restoring. NCCLs will be divided into two groups: a conventional restorative glass ionomer cement \[Fuji Bulk (GC, Tokyo Japan) (FB)\] and a posterior composite resin \[G-ænial Posterior (GC, Tokyo Japan) (GP)\] All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using modified United States Public Health Service (USPHS) criteria after a week (baseline) 6, 12, 24, 36 and 48 months. Descriptive statistics will be performed using chi-square tests.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Fuji Bulk | Restorative system |
| DEVICE | G-ænial Posterior | Restorative system |
Timeline
- Start date
- 2018-10-01
- Primary completion
- 2018-12-01
- Completion
- 2023-12-01
- First posted
- 2020-02-12
- Last updated
- 2025-03-10
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT04266210. Inclusion in this directory is not an endorsement.