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Clinical Trials/NCT06803537
NCT06803537Active, not recruitingNot Applicable

Three-Year Clinical Performance of Fiber-reinforced Versus Indirect Resin Composite Posterior Restorations

Mansoura University1 site in 1 country33 target enrollmentStarted: January 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
33
Locations
1
Primary Endpoint
FDI criteria for evaluation

Study Overview

Brief Summary

This study aimed to perform a comparison between the clinical performance of short fiber-reinforced composite and indirect lab composite restorations in posterior dentition.

Study Design

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

Eligibility Criteria

Ages
20 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients aged 20-35 year from both genders.
  • •Good oral hygiene: patients with low and moderate caries risk (according to Caries management by caries risk assessment CAMBRA sheets) were enrolled in this study.
  • •The visual examination should reveal the presence of a minimum of three primary occlusal or proximal caries (Black Class I and II) with a severity score of 4 or 5 according to the International Caries Detection and Assessment System (ICDAS).
  • •The carious teeth must exhibit vitality and do not display periapical radiolucency as evaluated by periapical radiography.
  • •The selected teeth must be under stable occlusion.

Exclusion Criteria

  • •Uncontrolled systemic disease
  • •Extremely poor oral hygiene
  • •Chronic periodontitis
  • •Heavy bruxism
  • •Cavities with a buccolingual width exceeding two-thirds of the intercuspal distance or requiring cusp covering.
  • •Patients undergoing orthodontic procedures.
  • •Patients unable to attend the scheduled recall appointments.

Arms & Interventions

Indirect lab composite

Active Comparator

Intervention: Fiber-reinforced composite (Other)

Indirect lab composite

Active Comparator

Intervention: Conventional resin composite (Other)

Conventional microhybrid resin composite

Active Comparator

Intervention: Fiber-reinforced composite (Other)

Conventional microhybrid resin composite

Active Comparator

Intervention: indirect lab composite (Other)

Fiber-reinforced composite

Active Comparator

Intervention: indirect lab composite (Other)

Fiber-reinforced composite

Active Comparator

Intervention: Conventional resin composite (Other)

Outcomes

Primary Outcomes

FDI criteria for evaluation

Time Frame: Three years follow-up

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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