Ignite Creation Date:
2024-05-06 @ 2:16 PM
Last Modification Date:
2024-10-26 @ 1:28 PM
Study NCT ID:
NCT04266210
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2023-08-22
First Post:
2020-02-10
Brief Title:
Clinical Evaluation of a Restorative Glass Ionomer and a Composite Resin for the Restoration
Sponsor:
Hacettepe University
Organization:
Hacettepe University
Study Overview
Official Title:
Clinical Evaluation Two Restorative Systems in Non-carious Cervical Lesions at Patients With Different Systemic Diseases
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2023-08
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:
The clinical performances of a restorative glass ionomer and a composite resin will be compared in the restoration of non-carious cervical lesions NCCLs at patients with systemic diseases
After recruiting participants with at least 2 NCCLs and at least one systemic disease all restorations will be placed by a single clinician All lesions will be cleaned before restoring
NCCLs will be divided into two groups a conventional restorative glass ionomer cement Fuji Bulk GC Tokyo Japan FB and a posterior composite resin G-ænial Posterior GC Tokyo Japan GP All restorative procedures will be conducted according to manufacturers instructions Restorations will be scored using modified United States Public Health Service USPHS criteria after a week baseline 6 12 24 36 and 48 months Descriptive statistics will be performed using chi-square tests
After recruiting participants with at least 2 NCCLs and at least one systemic disease all restorations will be placed by a single clinician All lesions will be cleaned before restoring
NCCLs will be divided into two groups a conventional restorative glass ionomer cement Fuji Bulk GC Tokyo Japan FB and a posterior composite resin G-ænial Posterior GC Tokyo Japan GP All restorative procedures will be conducted according to manufacturers instructions Restorations will be scored using modified United States Public Health Service USPHS criteria after a week baseline 6 12 24 36 and 48 months Descriptive statistics will be performed using chi-square tests
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