Evaluation of Marginal Integrity Using Bioactive Cement Incementation of Indirect Composite Blocks

Cairo University (CU)

Status and phase: Unknown; Phase 1

Conditions: Resin Cement

Treatments: Drug: Active bio Activa; Drug: Resin Cement

Study type: Interventional

Funder types: Other

Identifiers

NCT04557657

CEBD-CU-2019-07-17

Details and patient eligibility

About

The aim of this study is to evaluate of marginal integrity of indirect composite restoration after cementation by a bioactive cement in comparison to dual cure resin cement using Modified USPHS criteria

Full description

The study will be conducted in Conservative Dentistry Department, Faculty of Dentistry, Cairo University, The operator in charge will be: Mohamed Sherif . The researcher will bear ultimate responsibility for all activities associated with the conduct of a research project including recruitment of patients, explaining and performing the procedures to them,A total of 36 volunteer patients with Patients with badly broken vital teeth with minimum of two remaining walls. Patients will be randomly divided into two groups according to type of cement (S) where in group S1, Restoration will be cemented with resin cement ; while group S2,Restoration will be cemented with active cement. Each restoration will be assessed after three, six months and one year using modified USPH Criteria Marginal Discoloration, Recurrent Caries and Marginal Chipping with scale of Alpha and non alpha

Enrollment: 40 estimated patients

Sex: All

Ages: 16 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Patients with badly broken vital teeth with minimum of two remaining walls
• Adult Males or female 16- 65 years old
• Good oral hygiene measures with a good gingival condition
• Cooperative patients approving to participate in the study
• Free of any medical condition that interfere with procedures

Exclusion criteria

• Patients with a compromised medical history.
• Severe or active periodontal disease
• Endodontically treated teeth
• Severe medical complications Lack of compliance

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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40 participants in 2 patient groups

Control Group Resin cement

Experimental group

Description:

Control group Using resin cement

Treatment:

Drug: Resin Cement

Intervention Group Active Cement

Active Comparator group

Description:

Intervention Group Using active cement bio activa

Treatment:

Drug: Active bio Activa