Three year randomized clinical trial to evaluate the clinical performance of glass ionomer restorative systems in class I and II cavities
- Conditions
- The effect of glass ionomer in restoring posterior teethglass ionomerresin compositeclinical performanceposterior teeth
- Registration Number
- TCTR20201008001
- Lead Sponsor
- none
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 40
(1) a need for at least four posterior tooth-colored restorations in permanent premolars and molars, (2) small to medium sized primary carious lesions Class I or II, (3) the presence of teeth to be restored in contact with the adjacent teeth and in normal occlusion with the natural antagonist teeth, (4) symptomless vital teeth with
1) spontaneous pain or sensitivity to percussion, (2) partly erupted or endodontic treated teeth, (3) poor oral hygiene or severe periodontitis, (4) absence of neighboring or antagonist teeth, (5) adverse medical history, allergies or systemic diseases
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method fracture of material and retention 3 years clinical and radio-graphic evaluation
- Secondary Outcome Measures
Name Time Method surface luster 3 years magnifying aid