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Clinical Trials/NCT05418400
NCT05418400
Active, not recruiting
Not Applicable

Comparative Study of Clinical Criteria of Different Resin Composite Restorations Among Lower Molars

Al-Azhar University1 site in 1 country20 target enrollmentAugust 15, 2022
ConditionsDental Caries

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dental Caries
Sponsor
Al-Azhar University
Enrollment
20
Locations
1
Primary Endpoint
Post operative sensitivity
Status
Active, not recruiting
Last Updated
3 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
August 15, 2022
End Date
November 1, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mohamed Basha

principal investigator

Al-Azhar University

Eligibility Criteria

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.

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.

Outcomes

Primary Outcomes

Post operative sensitivity

Time Frame: along one year

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

recurrent caries

Time Frame: along one year

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

marginal adaptation

Time Frame: along one year

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

marginal discoloration

Time Frame: along one year

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

Study Sites (1)

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