Clinical Performance and Wear Mechanism of Hot-Pressed Ceramic Crowns

NCT ID: NCT00889239

Last Updated: 2015-05-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-05-31

Study Completion Date

2015-04-30

Brief Summary

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The objectives of this study are to characterize the clinical performance and wear mechanisms of all-ceramic posterior crowns. The wear rate of all-ceramic crowns and opposing enamel in selected patients will be quantified. The relationship of each subject's maximum clenching force and wear rate will also be analyzed.

Detailed Description

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High strength ceramics have been used in dentistry for constructing fixed partial denture. Their advantages are their acceptable fracture resistance, excellent biocompatibility, moderate opacity, etc. Because the increase in demand for more esthetic restoration, various ceramic materials have been used as a core material for several all-ceramic systems. Their properties have been investigated extensively in many in vitro studies. Currently, there are not much results regarding clinical performance and wear mechanism of ceramic-based prosthesis and more information are required for future research.

Conditions

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Ceramic and Dental Enamel Wear

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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A

ceramic crown

Group Type EXPERIMENTAL

lithia-disilicate-based crown

Intervention Type OTHER

all-ceramic crown

Interventions

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lithia-disilicate-based crown

all-ceramic crown

Intervention Type OTHER

Other Intervention Names

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ceramic crown

Eligibility Criteria

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Inclusion Criteria

* Occlusion: At least 20 remaining teeth for each patient, and at least one posterior endodontically treated tooth with natural opposing teeth
* Bruxism: No evidence based on an intraoral examination
* Dental history: No evidence of either moderate or severe periodontal disease
* Medical history: Good to excellent general health

Exclusion Criteria

* Periodontal status: Pocket depth greater than 4 mm
* Occlusion:

* Evidence of bruxism or excessive biting or clenching force
* Abutment tooth that opposes a removable partial denture
* Abutment tooth for fixed partial dentures
* Gingival recession of an abutment tooth more than 1 mm from the cementoenamel junction
* Tooth with first or second degree of tooth mobility
* Tooth with extensive carious lesions
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Thailand Research Fund

OTHER

Sponsor Role collaborator

Mahidol University

OTHER

Sponsor Role lead

Responsible Party

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Kallaya Suputtamongkol

Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Kallaya Suputtamongkol

Role: PRINCIPAL_INVESTIGATOR

Mahidol University

Locations

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Faculty of Dentistry, Mahidol University

Bangkok, , Thailand

Site Status

Countries

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Thailand

Other Identifiers

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MRG 4780066

Identifier Type: -

Identifier Source: org_study_id

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