Ignite Creation Date:
2024-10-25 @ 8:02 PM
Last Modification Date:
2024-10-26 @ 3:38 PM
Study NCT ID:
NCT06572124
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-08-23
Brief Title:
Clinical Performance of ARS Containing Universal Adhesives in Carious Cervical Lesions
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Clinical Performance of Universal Adhesive with and Without Acid Resistant Silane Coupling Agent in Carious Cervical Lesions A Randomized Controlled Trial
Status:
NOT_YET_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:
Evaluation of composite restorations done in carious cervical lesions restored by a conventional universal adhesive in comparison to a universal adhesive that contains and resistant silane coupling agent according to the Modified United States Public Health Service USPHS criteria over 18 months
Detailed Description:
The presence of acidic monomers in the bottle during storage can lead to the hydrolysis of silane contained in universal adhesives potentially reducing its effectiveness and causing instabilityThe acid resistant silane coupling agent has a protective structure against attacks from acidic monomers Therefore long-term storage stability can be expected by suppressing hydrolysis The protective structure is removed when the concentration of acidic monomers increases by air drying after application This activates ARS exerting the silane coupling effect
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