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Clinical Evaluation of Different Resin Composite Restorations

Not Applicable
Active, not recruiting
Conditions
Dental Caries
Interventions
Other: sonic fill 3 & PALFIQUE bulk flow & Neo spectra & Clear fill AP-X
Registration Number
NCT05418400
Lead Sponsor
Al-Azhar University
Brief Summary

Posterior resin composite is challenging esthetic restoration. Patients seek for durable, esthetic and functional restorations in molars. one of the major problems is polymerization shrinkage. Some materials were developed to overcome the polymerization shrinkage, among them bulk fill resin composite which have been developed to reduce the shrinkage stress during polymerization and offer much greater depth of cure. This is achieved by the addition of fillers such as barium aluminum silicate filler, ytterbium trifluoride and mixed oxides. Furthermore, a prepolymerized fillers have been added with silanes to reduce shrinkage stress. so, the objective of this trial is to clinical Evaluate and compare clinical performance of bulk fill VS incremental filling technique.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
20
Inclusion Criteria

inclusion criteria of participants:

  • Male gender
  • Good oral hygiene
  • Only Cooperative patient
  • Medically free patient
  • Age range 18-24

inclusion criteria of the teeth:

  • Vital teeth with no periapical lesion or radiolucency.
  • Prepared cavity with no undermined enamel walls.
  • Functioning tooth with presence of an opposing.
  • Healthy periodontium.
Exclusion Criteria
  • exclusion criteria of participants:

    • Old age patients
    • Patients have systemic disease or sever medically compromised
    • Patients with bruxism, clenching or temporomandibular joint disorder.
    • Por oral hygiene

exclusion criteria of teeth:

  • Teeth with periapical lesions.
  • Teeth with visible cracks.
  • Teeth with mobility.
  • Non-functioning tooth with no opposing tooth.
  • Heavy occlusion or signs of sever attrition.
  • Tooth with Periodontal affection.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
bulkfill compositessonic fill 3 & PALFIQUE bulk flow & Neo spectra & Clear fill AP-Xsonic fill 3 \& PALFIQUE bulk flow bulk fill composite
incremental compositessonic fill 3 & PALFIQUE bulk flow & Neo spectra & Clear fill AP-XNeo spectra \& Clear fill AP-X incremental composites
Primary Outcome Measures
NameTimeMethod
Post operative sensitivityalong one year

restorations will be evaluated the according to the modified United States Public Health Service (USPHS)

recurrent cariesalong one year

restorations will be evaluated the according to the modified United States Public Health Service (USPHS)

marginal adaptationalong one year

restorations will be evaluated the according to the modified United States Public Health Service (USPHS)

marginal discolorationalong one year

restorations will be evaluated the according to the modified United States Public Health Service (USPHS)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Faculty of dental medicine Al Azhar university

🇪🇬

Cairo, Egypt

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