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Influence of Resin Cement Composition on the Longevity of Intraradicular Post of Endodontically Treated Teeth

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03491527
Enrollment
20
Registered
2018-04-09
Start date
2018-05-01
Completion date
2019-07-30
Last updated
2018-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

MTA, Endodontically Treated Teeth, Resin Cement

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.

Interventions

Absolute isolation with rubber dam

PROCEDUREManipulation of the resin cement with MTA

Manipulation of the resin cement with MTA according to the manufacturer's recommendations.

PROCEDUREManipulation of the resin cement without MTA

Manipulation of the resin cement without MTA according to the manufacturer's recommendations.

PROCEDUREFiber Post cimentation

Insertion of the cement on the root canal and on post surface. Light-cured for 40 seconds on each surface.

PROCEDUREDental Prepare

Confection of a indirect crown prepare with diamand burs.

PROCEDUREDental impression

Dental impression whith silicone.

PROCEDURECrown cimentation

Insertion of the cement on the inner surface of the crown. Light-cured for 40 seconds on each surface.

Analysis of the occlusion with carbon paper.

Sponsors

Federal University of Uberlandia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
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.1 year

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026