Trials / Recruiting
RecruitingNCT04533113
Carious Tissue Selective Removal on Permanent Posterior Teeth.
Carious Tissue Selective Removal on Permanent Posterior Teeth. A Randomized Controlled Clinical Study.
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 111 (estimated)
- Sponsor
- Juan Gonzalo Olivieri · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Accepted
Summary
This study is a prospective randomized controlled study of patients who come to the University. The aim is to evaluate the success rate of selective removal of carious tissue in deep lesions of posterior teeth. Three different materials will be used as liners (VitreBond ™Plus, BioDentine™, and Theracal™ LC). Post-operative pain, clinical, and radiographic success will be evaluated at one, two, and five-year follow-up. The null hypothesis is that there will be no statistically significant differences in rates of successful treatment with the three materials used.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Carious tissue selective removal | Carious tissue selective removal in deep carious lesions in posterior teeth, using one of three materials as a liner under the final composite restoration |
Timeline
- Start date
- 2019-02-20
- Primary completion
- 2021-07-01
- Completion
- 2026-07-01
- First posted
- 2020-08-31
- Last updated
- 2020-08-31
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT04533113. Inclusion in this directory is not an endorsement.