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Clinical Trials/NCT03491527
NCT03491527
Unknown
Not Applicable

Influence of Resin Cement Composition on the Longevity of Intraradicular Post in the Rehabilitation of Endodontically Treated Teeth - Randomized Clinical Trials

Federal University of Uberlandia1 site in 1 country20 target enrollmentMay 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
MTA
Sponsor
Federal University of Uberlandia
Enrollment
20
Locations
1
Primary Endpoint
Success rate (post or dental crown displacement; fracture of the core/post/crown; marginal integrity and absence of endotontic alterations) of definitive indirect crowns with a 1 year follow up.
Last Updated
8 years ago

Overview

Brief Summary

The aim of this study is through a randomized clinical trial, double blind, splithmouth, evaluate the success rate (post or dental crown displacement; fracture of the core/post/crown; marginal integrity and absence of endotontic alterations) of definitive indirect crowns un endodontically treated teeth. The composition of the resin cement (with and without mineral trioxide aggregate) will be evaluated. Data will be collected, tabulated and submitted to statistical analysis.

Detailed Description

Endodontically treated teeth present an increased risk of fracture and are usually related to extensive carious processes or trauma that promote major coronary destruction. In such situations, it may be necessary to indicate intra-radicular retainers, such as fiberglass pins, to retain the restorative material. The aim of this study is through a randomized clinical trial, double blind, splithmouth, evaluate the success rate (post or dental crown displacement; fracture of the core/post/crown; marginal integrity and absence of endotontic alterations) of definitive indirect crowns un endodontically treated teeth. The composition of the resin cement (with and without mineral trioxide aggregate) will be evaluated. Twenty participants with at least two teeth with endodontic treatment with need intraradicular post cementation and confection of indirect dental crown (each participant) will be selected. The teeth will be randomly divided into 2 different groups according to resin cement composition (with and without mineral trioxide aggregate). Data will be collected, tabulated and submitted to statistical analysis.

Registry
clinicaltrials.gov
Start Date
May 1, 2018
End Date
July 30, 2019
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Federal University of Uberlandia
Responsible Party
Principal Investigator
Principal Investigator

PAULO VINICIUS SOARES

Director of NCCL Research Group

Federal University of Uberlandia

Eligibility Criteria

Inclusion Criteria

  • Healthy volunteers;
  • Presence of at least two teeth with endodontc treatment;
  • Presence of at least two teeth with indication of total crowns;
  • Good oral hygiene.

Exclusion Criteria

  • Dentures or orthodontics;
  • Presence of periodontal disease
  • Presence of parafunctional habits
  • Presence of systemic disease
  • Constant use of analgesic and or anti-inflammatory
  • Allergic response to dental products

Outcomes

Primary Outcomes

Success rate (post or dental crown displacement; fracture of the core/post/crown; marginal integrity and absence of endotontic alterations) of definitive indirect crowns with a 1 year follow up.

Time Frame: 1 year

Study Sites (1)

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