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Completed

NCT Number: NCT07415317

Influence of Composite Placement Techniques on the Clinical Performance of Posterior Restorations in Vital Teeth

The purpose of this 12-month randomized clinical investigation was to compare the clinical performance of posterior composite resin restorations implanted in vital teeth using various placement techniques.

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Key information

Age range

20 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Restorative Department, Faculty of Dentistry, Tanta University, Tanta, Egypt

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About this study

Because of their conservative nature, aesthetic qualities, and consistently improved mechanical performance and handling features, resin-based composites have become the restorative material of choice for posterior teeth. Nevertheless, significant obstacles influencing the stability of the marginal area, sensitivity following the procedure, and the durability and effectiveness of composite restorations in the long run are polymerization shrinkage and stress associated with shrinkage.

To reduce polymerization stress and maximize adaptability to hollow walls, various placement procedures have been suggested. While older incremental layering methods sought to lessen the configuration factor (C-factor) and increase light penetration, more recent methods like the Stamp and Snowplow approaches sought to replicate the occlusal architecture and enhance marginal sealing. Conversely, bulk-fill techniques were first developed to streamline clinical processes by enabling the use of bigger composite layers with the promise of lower shrinkage stress.

Despite a plethora of in vitro studies, there is a dearth of high-quality clinical data that compares these placement methods under controlled settings. Due to the fact that laboratory studies cannot completely replicate the oral environment, clinical trials continue to be the best way to assess the real-world efficacy of restorative procedures.

Consequently, this randomized clinical trial set out to assess the clinical efficacy of posterior composite restorations placed in vital teeth utilizing four distinct procedures over the course of a year

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Good general and oral health
  • Vital posterior teeth with primary occlusal caries
  • Class I cavities with depth ranging from 3 to 4 mm

Exclusion criteria

  • Non-vital or restored teeth
  • Parafunctional habits (e.g., bruxism)

Treatment and study plan

nanohybrid composite resin

Other

Fifty patients received a total of 200 Class I composite restorations, which were placed using the same nanohybrid composite resin and randomly allocated into four groups (n = 50) according to placement technique: Group I-Stamp technique; Group II-Snowplow technique; Group III-Modified incremental "Pizza" technique; and Group IV-Bulk-fill technique

Primary outcomes

  1. The primary outcome was marginal adaptation

    Time frame: 24 months

    Clinical evaluation of marginal adaptation was performed according to the World Dental Federation (FDI) by two calibrated evaluators at baseline and at 6, 12, and 24 months. All of the restorations were ranked according to how well they met the criteria: score 1 (clinically excellent), score 2 (clinically satisfactory), score 3 (clinically satisfactory), or scores 4 and 5 (clinically inadequate). Clinical success was defined as a score of 1, 2, or 3, and failure was indicated by scores of 4 or 5. A powerful light source was used to conduct the visual inspection of the parameters. A magnifying dental loupe was utilized for this purpose. The Friedman test was conducted to evaluate intragroup comparisons of the same restoration outcomes through different follow-up periods. The Kruskal-Wallis test was utilized to assess intergroup comparisons between different restorations during the same follow-up period.

    Time Frame: 24 months

Sponsors and collaborators

Lead sponsor

Tanta University

Other

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Feb 17, 2026
Registry last updated
Feb 17, 2026

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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