IRCT138709301509N1
Completed
Phase 3
Clinical evaluation of three adhesive systems for the restoration of non-carious cervical lesions
Vice-chancellor for Research, Mashhad and Tabriz Universities of Medical Sciences.0 sites90 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Condition 1: Noncarious cervical lesions. Condition 2: Noncarious Cervical Lesions.
- Sponsor
- Vice-chancellor for Research, Mashhad and Tabriz Universities of Medical Sciences.
- Enrollment
- 90
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Inclusion Criteria: Age 20 to 50 years, signing informed consent prior to commencement of any treatment, Presence of at least have three NCCLs, having contact with opposite teeth without any high occlusion stress for selected teeth, cavity cervical margins placed on cementum with no more than 50% put on enamel, assessable isolation and observable and easily accessible gingival margins during tooth restoration,
Exclusion Criteria
- •Any systemic disease, any periodontal disease, history of periodontal surgery three months prior to study, poor oral hygiene, treatment with anti sensitivity materials such as desensitizer dentifrices, high\-risk caries, cervical lesions with caries and restricted to the labial area with extending to proximal surfaces, cervical lesions with severe degree of sclerosis, presence of any caries or restorations except in cervical area of the tooth labial portion, the deep of cervical lesion more than 2 mm (probe measurement), depth of lesion more than usual that need to liner placement such as calcium hydroxide.
Outcomes
Primary Outcomes
Not specified
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