Clinical Performance of ARS Containing Universal Adhesives in Carious Cervical Lesions
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-67
SponsorCairo University
About this trial
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.
Eligibility criteria
Qualifiers
Vital teeth with carious cervical lesions in incisors , canines ,premolars& molars
Disqualifiers
Patients with fewer than 20 teeth
Poor oral hygiene
Uncontrolled periodontal disease
Xerostomia
Trial design
Treatments tested in this trial
- universal adhesive without Acid resistant silane coupling agent
- universal adhesive with Acid resistant silane coupling agent
Treatment groups
80 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov