CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 240 enrolled
Drug / intervention
Filtek™ Bulk Fill Posterior Restorative +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03764059
NCT03764059N/ACompleted
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A Randomized Multicenter Two-Arm Clinical Study to Evaluate the Safety and Efficacy of Filtek™ Bulk Fill Posterior Restorative in Class I and II Restorations

3M·interventional·Posted Dec 4, 2018·Updated Jul 21, 2023

In Brief

A clinical study evaluating Filtek™ Bulk Fill Posterior Restorative and Filtek™ Z350XT Universal Restorative for Dental Caries Class I and Dental Caries Class II. Completed, enrolled 240 participants across 3 sites.

Detailed Summary

Purpose of the Study:This study was to evaluate the 1 week, 1 year safety and effectiveness of dental composite resin (Filtek™ Bulk Fill Posterior Restorative) in restoring Class I and II dental cavities in posterior teeth.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDental Caries Class I, Dental Caries Class II
CountriesChina
Collaborators--

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedDec 4, 2018
Enrollment StartOct 17, 2017
Primary CompletionNov 14, 2019
TodayJul 2, 2026
Enrollment to primary: 2.1 yearsPosted 7.6 years ago

Interventions

Filtek™ Bulk Fill Posterior Restorativedevice

The subjects were assigned to either the investigational device (Filtek™ Bulk Fill Posterior Restorative) or the control device (Filtek™ Z350XT Universal Restorative) per web-based randomization system.

Filtek™ Z350XT Universal Restorativedevice

The subjects were assigned to either the investigational device (Filtek™ Bulk Fill Posterior Restorative) or the control device (Filtek™ Z350XT Universal Restorative) per web-based randomization system.