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OpenTrials
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NCT Number: NCT06803537

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

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

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Conditions

Occlusal Caries Proximal Caries

Age range

20 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mansoura university

Al Mansurah, Dakahlia Governorate, 35516, Egypt

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Fiber-reinforced composite

Other

short fiber-reinforced composite used as base covered by conventional composite

indirect lab composite

Other

indirect lab processed resin composite inlay restorations

Conventional resin composite

Other

conventional microhybrid resin composite posterior restorations

Primary outcomes

  1. FDI criteria for evaluation

    Time frame: Three years follow-up

Sponsors and collaborators

Lead sponsor

Mansoura University

Other

Registry information

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Jan 31, 2025
Registry last updated
May 11, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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