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Clinical Trials/IRCT138709301509N1
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Vice-chancellor for Research, Mashhad and Tabriz Universities of Medical Sciences.

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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