Short Fiber vs Injectable Resin Composite in Class I Restorations
Summary
NIH ClinicalTrials.gov registered a Phase 4 clinical trial (NCT07535086) comparing short fiber reinforced flowable bulk fill resin composite to conventional injectable flowable resin composite for restoring Class I carious molar cavities. The trial will evaluate clinical performance of these dental restoration materials. Estimated study completion date is April 16, 2026.
What changed
A new clinical trial has been registered on ClinicalTrials.gov (NCT07535086) to evaluate the clinical performance of short fiber reinforced flowable bulk fill resin composite versus conventional injectable flowable resin composite in Class I carious cavity restorations. The trial will restore carious molars with these different materials to compare outcomes.
For dental manufacturers and healthcare providers, this trial represents an informational registration comparing dental restoration materials. No compliance obligations or regulatory actions are associated with this document. The trial is categorized as Phase 4 (post-market surveillance) and involves interventions including an experimental version of flowable fiber reinforced bulk fill resin composite and light curing devices.
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Archived snapshot
Apr 16, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
Clinical Performance of Short Fiber Reinforced Flowable Versus Conventional Injectable Flowable Resin Composite Restorations in Class I Carious Cavities
N/A NCT07535086 Kind: NA Apr 16, 2026
Abstract
Investigators will restore carious molar with different restoring materials for comparison
Conditions: Restoration of Posterior Teeth
Interventions: updating experimental version of flowable fiber reinforced bulk fill resin composite, Fiber reinforced flowable resin composite, light curing device
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