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NOT YET RECRUITING
NCT06572124
NA

Clinical Performance of ARS Containing Universal Adhesives in Carious Cervical Lesions

Sponsor: Cairo University

View on ClinicalTrials.gov

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.

Official title: Clinical Performance of Universal Adhesive with and Without Acid Resistant Silane Coupling Agent in Carious Cervical Lesions :A Randomized Controlled Trial

Key Details

Gender

All

Age Range

21 Years - 67 Years

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2024-09-01

Completion Date

2026-04-30

Last Updated

2024-09-04

Healthy Volunteers

Yes

Interventions

PROCEDURE

universal adhesive without Acid resistant silane coupling agent

After 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.

PROCEDURE

universal adhesive with Acid resistant silane coupling agent

After 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.

Locations (1)

Cairo University

Cairo, Egypt