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Clinical Trials/NCT05418400
NCT05418400Active, not recruitingNot Applicable

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

Al-Azhar University1 site in 1 country20 target enrollmentStarted: August 15, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
20
Locations
1
Primary Endpoint
Post operative sensitivity

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 24 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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.

Arms & Interventions

bulkfill composites

Active Comparator

sonic fill 3 & PALFIQUE bulk flow bulk fill composite

Intervention: sonic fill 3 & PALFIQUE bulk flow & Neo spectra & Clear fill AP-X (Other)

incremental composites

Active Comparator

Neo spectra & Clear fill AP-X incremental composites

Intervention: sonic fill 3 & PALFIQUE bulk flow & Neo spectra & Clear fill AP-X (Other)

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)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mohamed Basha

principal investigator

Al-Azhar University

Study Sites (1)

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