Resin Modified Glass Ionomer Versus Self-Adhesive Resin Composite Restorative Systems
Recruiting
N/A
Interventional Study
Secondary Caries Dental Restoration Failure of Marginal Integrity
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 30 – 60
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 35 (estimated)
- Sponsor
- Mansoura University · Other
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About This Trial
To evaluate and compare two-year clinical performance of commercially available resin modified glass ionomer cement, self-adhesive composite hybrid and self-adhesive flowable composite restorative materials for non-carious cervical lesions
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Inclusion criteria will be fair oral hygiene patients with 30-60 years. Patients with at least three similarly sized non-carious cervical lesions (NCCLs) in vital teeth that need for restoration and depth of NCCLs will be 1-3 mm with at least 50% of margins without enamel.
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