Ignite Creation Date:
2024-05-06 @ 8:28 PM
Last Modification Date:
2024-10-26 @ 3:28 PM
Study NCT ID:
NCT06393270
Status:
COMPLETED
Last Update Posted:
2024-05-01
First Post:
2024-04-24
Brief Title:
5-year Clinical Follow-up of Restorative Materials
Sponsor:
Selcuk University
Organization:
Selcuk University
Study Overview
Official Title:
5-year Clinical Follow-up of Bulk-fill Restorative Materials in Class II Restorations
Status:
COMPLETED
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Materials to be used as permanent filling materials in Class II restorations are still an essential field of study This study aims to evaluate the 5-year clinical performance of Class II restorations performed with different bulk-fill restorative materials
The study was planned as an observational clinical trial In the study Class II restorations performed with Tetric Bulk Fill TBF and Filtek Bulk Fill FBF composites and Equia Forte Fil EF will be evaluated Fifty-one patients and 119 restorations will be included in the study Restorations will be assessed in terms of modified United States Public Health Service USPHS criteria during the 5th year Cochran Q Pearson chi-square and Fisher-Freeman-Halton tests will be used for statistical analysis
The study was planned as an observational clinical trial In the study Class II restorations performed with Tetric Bulk Fill TBF and Filtek Bulk Fill FBF composites and Equia Forte Fil EF will be evaluated Fifty-one patients and 119 restorations will be included in the study Restorations will be assessed in terms of modified United States Public Health Service USPHS criteria during the 5th year Cochran Q Pearson chi-square and Fisher-Freeman-Halton tests will be used for statistical analysis
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None