Clinical Performance of One-shade Universal Dental Resin Composite as Posterior Restoration

Minia University

Status: Completed

Conditions: Carious Teeth

Treatments: Other: US Public Health Service "USPSH" criteria for assessment of success of resin composite restorations

Study type: Interventional

Funder types: Other

Identifiers

NCT05500547

RSAnwar

Details and patient eligibility

About

This study is aimed to evaluate the clinical performance of new One-shade universal composite resin as posterior restoration using US Public Health Service "USPSH" criteria for color match, marginal adaptation, surface texture, retention, recurrent caries and others after 1, 3, 6 and 9 months.

Full description

One operator will place all restorations under rubber-dam isolation. The patients will receive restorations with both materials, randomly after shade selection (The shade of single shade universal resin composite "Omnichroma" will be taken before and after placement into the cavity). During the referred period, only the two composites in study will be placed in posterior teeth in the dental office. The various materials' application procedure will be applied according to manufacturer's instructions.

Enrollment: 40 patients

Sex: All

Ages: 25 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• • They should have an acceptable oral hygiene level.

  • Presence of at least two occlusal carious lesions to be restored with two different types of composite.
  • The two studied materials restorations should be used in approximately the same sized lesions or within the same extension.
  • Age range between 25 and 45years.

Exclusion criteria

• • Severe or active periodontal or carious disease and heavy bruxism or a traumatic occlusion

  • Patients with a compromised medical history, or had received therapeutic irradiation to the head and neck region.
  • Alcoholic and smoker patients.
  • Patients had participated in a clinical trial within 6 months before commencement of this trial.
  • Patients unable to return for recall appointment

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

---

40 participants in 2 patient groups

Universal single shade resin composite restorative material

Experimental group

Description:

Dental restorative material

Treatment:

Other: US Public Health Service "USPSH" criteria for assessment of success of resin composite restorations

Nano-hybrid multi-shade resin composite restorative material

Active Comparator group

Description:

Dental restorative material

Treatment:

Other: US Public Health Service "USPSH" criteria for assessment of success of resin composite restorations