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Trials / Not Yet Recruiting

Not Yet RecruitingNCT06572124

Clinical Performance of ARS Containing Universal Adhesives in Carious Cervical Lesions

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
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
21 Years – 67 Years
Healthy volunteers
Accepted

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 instability,The 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.

Conditions

Interventions

TypeNameDescription
PROCEDUREuniversal adhesive without Acid resistant silane coupling agentAfter cavity preparations, enamel margins will be etched for 30 seconds then rinsed and dried, then the Universal adhesive without acid resistant silane coupling agent will be actively applied for 20 seconds then air thinned for 5 seconds then cured for 20 seconds.Then the composite restoration will be placed.
PROCEDUREuniversal adhesive with Acid resistant silane coupling agentAfter cavity preparations, enamel margins will be etched for 30 seconds then rinsed and dried, then the Universal adhesive which contains acid resistant silane coupling agent will be actively applied for 20 seconds then air thinned for 5 seconds then cured for 20 seconds.Then the composite restoration will be placed.

Timeline

Start date
2024-09-01
Primary completion
2026-04-30
Completion
2026-04-30
First posted
2024-08-26
Last updated
2024-09-04

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06572124. Inclusion in this directory is not an endorsement.