Ignite Creation Date:
2024-10-25 @ 8:03 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06543680
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-08-04
Brief Title:
Resin Modified Glass Ionomer Versus Self-Adhesive Resin Composite Restorative Systems
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Resin Modified Glass Ionomer Versus Self-Adhesive Resin Composite Restorative Systems Two Years Randomized Clinical Study in Class ᴠ
Status:
RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
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
Detailed Description:
The experimental design description adhered to the guidelines provided by the Consolidated Standards of Reporting Trials CONSORT statement The present study is planned as a double-blinded randomized clinical trial ensuring that both the patients and the examiner are unaware of the treatment allocation The trial will follow a parallel design A total of 35 patients who are seeking dental treatment will be enrolled in the study The participants will be recruited from the Operative Department clinic at the Faculty of Dentistry University of Mansoura The study will focus on 105 Class V restorationsA randomized clinical trial will be performed A number of 35 patients will be included in this study Each patient will have at least three NCCLs One of these lesions will be randomly restored with resin modified glass ionomer cement the second lesion will be restored with self-adhesive Surefil One composite hybrid while the third lesion will be restored with self-adhesive flowable composite
No active advertisement will be used for participant recruitment and instead a convenience sample will be formed Prior to participating in the study each patient will be required to provide informed consent by signing a consent form The study is scheduled to be conducted from may 2023 to may 2025 The form and protocol of the study will be approved by Mansoura Universitys ethics committee before initiation
Clinical evaluation for all restorations will be done at baseline after insertion and after 6 12 and 24 months of clinical service by two calibrated independent examiners that will not share in restorations placement It will be designed depending on modified USPHS criteria and FDI criteria
No active advertisement will be used for participant recruitment and instead a convenience sample will be formed Prior to participating in the study each patient will be required to provide informed consent by signing a consent form The study is scheduled to be conducted from may 2023 to may 2025 The form and protocol of the study will be approved by Mansoura Universitys ethics committee before initiation
Clinical evaluation for all restorations will be done at baseline after insertion and after 6 12 and 24 months of clinical service by two calibrated independent examiners that will not share in restorations placement It will be designed depending on modified USPHS criteria and FDI criteria
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None