Clinical Evaluation of Bulk-fill Alkasite Restoration Versus Resin Modified Glass Ionomer in Adult With Class V Carious

Cairo University (CU)

Status

Unknown

Conditions

Cervical Lesion

Treatments

Other: Alkasite bioactive restorative material.

Other: Resin Modified Glass Ionomer

Study type

Interventional

Funder types

Other

Identifiers

NCT04716517

381020

Details and patient eligibility

About

Cention N will have the same clinical performance as resin-modified glass ionomer in cervical carious lesions. Evaluation of restorations will be done at baseline, six months, and one year according (USPHS) criteria.

Full description

In this study, Class V carious lesions were restored using two different restorative materials either resin modified glass ionomer or Cention N restorative materials. This study will be held in the restorative clinic at Future University in Egypt. Patients will be assessed for medical and dental histories first. Then an examination of the patients will be done using visual inspection by using a dental mirror and probe. Eligible patients according to inclusion and exclusion criteria will be informed about all procedures with follow up time if they accept, 12 their signature on written informed consents will be obtained. Eligible participants will be randomly divided into two groups according to the type of restoration they will be received. The first group (A) will be received resin modified glass ionomer restorative material and the second group (B) will be received Cention N restorative materials. Each restoration will be evaluated for clinical parameters after finishing and polishing at baseline and regular recalls of 6 months and one year.

The restorations will be clinically examined according to modified USPHS criteria in terms of marginal adaptation, anatomic form, color match, marginal discoloration, secondary caries, postoperative sensitivity and retention. The information that will be obtained will be collected and statistically analyzed

Enrollment

28 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Patients with High caries risk.
Patients with poor oral hygiene.
Patients with untreated cervical caries lesion.
patient aging ≥18 years.
Absence of tooth mobility
Absence of abnormal occlusion.
Patients with good likelihood of recall availability.

Exclusion criteria

Patients with cervical caries lesions need crown restoration.
Non-vital teeth.
Evidence of parafunctional habits.
Teeth supporting removable prosthesis.
Periapical Abscess or Fistula.
Patients with systemic disease.
Patients with xerostomia.
Participants with a history of allergy to any component of restorations will be used in the study.