Overview

This trial is active, not recruiting.

Conditions dental caries, restorative material
Treatments urethane dimethacrylate, tph3
Sponsor University of Rochester
Start date June 2013
End date December 2017
Trial size 50 participants
Trial identifier NCT02018822, 765-552

Summary

This double blind randomized controlled prospective clinical trial will compare the clinical success of two tooth colored resin composite dental filling materials - TPH3 (Dentsply Caulk) and an experimental urethane dimethacrylate resin based composite resin (Dentsply Caulk) for wear resistance, staining and marginal seal using modified Ryge criteria to evaluate the posterior restorations for 24 months in duration

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification efficacy study
Intervention model parallel assignment
Masking double blind (subject, investigator)
Primary purpose treatment
Arm
(Active Comparator)
TPH3
tph3
(Experimental)
urethane dimethacrylate
urethane dimethacrylate

Primary Outcomes

Measure
Evaluate a composite resin
time frame: 24 months

Eligibility Criteria

Male or female participants from 18 years up to 85 years old.

Inclusion Criteria:• must have given written consent to participate in the trial - must be in need of at least two restorations in natural tooth - replacement restorations with or without caries are acceptable - must be available for the required post-operative follow-up visits - restorations to be in bicuspids, 1st or 2nd molars - restorations to be in contact with opposing natural or crowned teeth - class II restorations must have at least one proximal contact - restorations must have a buccal to lingual/palatal width equal to or greater than 1/3 the distance from buccal to lingual/palatal cusp tips - 75% of the restorations must be Class II - all restorations must have at least one occlusal contact in habitual closure Exclusion Criteria: - have severe medical complications (organ transplants, long term antibiotic or steroid treatment, cancer or immunocompromised) or disabilities who may not be able to tolerate the time required to complete the restorations or to provide adequate oral hygiene - have xerostomia either by taking medications known to produce xerostomia or those with radiation induced or Sjogren's syndrome patients - have chronic periodontitis, rampant caries or poor oral hygiene which may require extraction of the teeth to be restored - have a history of chronic bruxism and those unavailable for long term recall - can not tolerate the rubber dam required for tooth isolation during preparation and restoration. - do not meet all inclusion criteria - present with any systemic or local disorders that contra-indicate the dental procedures included in this study - have an unstable occlusion - have severe bruxing or clenching or need of TMJ related therapy - have teeth with periapical pathology or expected pulp exposures - have teeth that are non-vital or that exhibit signs of pulpal pathology - Pregnancy - Known sensitivity to methacrylates and/or acrylates

Additional Information

Official title Clinical Evaluation of an Experimental Urethane Dimethacrylate Resin Based Composite
Description The purposes of this clinical trial is to evaluate two composite resins used to restore Class I and Class II cavities in teeth of adults. The clinical study will evaluate the resin composite restorations placed in Class I and Class II cavity preparations for anatomic form, color match, marginal integrity, marginal discoloration, proximal contact, polishability, caries, sensitivity, gingival index, staining,wear, and thermal response for 24 months..
Trial information was received from ClinicalTrials.gov and was last updated in September 2016.
Information provided to ClinicalTrials.gov by University of Rochester.