Wear of Vita Ambria Only Restoration Compared With IPS Emax Onlay Restoration

Al-Azhar University

Status: Enrolling

Conditions: Carious Tooth; Dental Wear

Treatments: Other: Vita Ambria; Other: IPs emax onaly

Study type: Interventional

Funder types: Other

Identifiers

NCT05431465

Wear of Vita Ambria

Details and patient eligibility

About

The 1ry objective will be to evaluate the amount of wear of onlays restorations made from VITA AMBRIA & IPS e.max Press and their opposing natural teeth.

2. The 2ry objective of the clinical trial will be to evaluate the fractures, retention, contact points, food impaction and radiographic examination of the VITA AMBRIA onlays compared with IPS e.max press onlays as defined by FDI criteria.

Full description

A randomized controlled clinical trial, a double-blind (patient and examiner) is conducted by one trained and calibrated operators who perform all restorative procedures. The restorations are evaluated by a blind and calibrated two examiner using the FDI World Dental Federation criteria. A total of 24 patients will be randomly assigned to each group for a total of 48 patients. The randomization sequence will be generated (www.randomlists.com/team-generator) and to ensure the confidentiality of the allocation, this will be used opaque, sealed and numbered envelopes in series. These will be kept with an independent researcher for the moment of inclusion of the subjects.

Both groups will receive Onlay preparation . Digital impression by intra oral scanner will be taken, wax pattern for the onlay restoration will be designed and milled using CAD/CAM software. After that, the wax pattern will be invested and final onlay restoration will be constructed from VITA AMBRIA and IPS e.max press ingots according to manufacturing instructions. Primary outcome: The amount of wear will be evaluated according to FDI standard.

Enrollment: 48 estimated patients

Sex: All

Ages: 18 to 50 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• The patient is healthy.
• 18-50 years old.
• Normal occlusion.
• Good oral hygiene.
• Tooth with complete root apex.
• Tooth with moderate coronal decay.

Exclusion criteria

• Patient Incapable of self-care, mental illness, undergoing radiotherapy, diabetic patient, allergy to one of the materials used, pregnancy, smoker, parafunctional habits, poor oral hygiene, severe periodontitis, tooth need vital pulp therapy or surgical crown lengthening or marginal elevation, tooth with enamel or dentin hypoplasia or hypocalcification, Mallaligned or malformed teeth and adjacent or opposing teeth are missed.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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48 participants in 2 patient groups

Vita Ambria onlay

Experimental group

Description:

The onlays will be constructed from Zirconia reinforced Lithium disilicate (Vita Ambria) glass ceramic system.

Treatment:

Other: Vita Ambria

IPS emax onlay

Active Comparator group

Description:

The onlays will be constructed from Lithium disilicate (IPS e-max press) glass ceramic system

Treatment:

Other: IPs emax onaly