Aesthetic Evaluation of Different Abutment Materials for OsseoSpeed Implants

NCT ID: NCT02090647

Last Updated: 2014-03-18

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

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-01-31

Study Completion Date

2014-01-31

Brief Summary

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The objective of the study was to assess the aesthetic outcome of different abutments materials and shapes on dental implants .

A set of parameters, including assessments of the mucosa and periodontal tissue , soft tissue , radiographic evaluations and clinical photographs, was used to obtain a measure of the aesthetic of implant-prosthesis rehabilitations.

Detailed Description

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Conditions

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Aesthetic Evaluation Implant Survival Rate

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Investigators

Study Groups

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titanium 1

titanium abutment type 1

Group Type ACTIVE_COMPARATOR

aesthetic outcome

Intervention Type BEHAVIORAL

titanium 2

titanium abutment type 2

Group Type ACTIVE_COMPARATOR

aesthetic outcome

Intervention Type BEHAVIORAL

zirconia 1

zirconia abutment type 1

Group Type ACTIVE_COMPARATOR

aesthetic outcome

Intervention Type BEHAVIORAL

zirconia 2

zirconia abutment type 2

Group Type ACTIVE_COMPARATOR

aesthetic outcome

Intervention Type BEHAVIORAL

titanium nitrate

titanium nitrate abutment

Group Type ACTIVE_COMPARATOR

aesthetic outcome

Intervention Type BEHAVIORAL

Interventions

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aesthetic outcome

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* aged over 18 years
* dental implant rehabilitation requested
* at least 1 tooth missing in areas between 1.5-3.5 and 3.5-4.5
* sufficient bone volume for implant placement ( length 10-15mm; diameter 2.5-4mm, bone quality between class I and III of Lekholm and Zarb).
* informed consensus acceptance

Exclusion Criteria

* systemic pathologies that represent controindication to implantology
* smoking (more than 10 cigarettes per day)
* severe bruxism
* untreated periodontitis
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Siena

OTHER

Sponsor Role lead

Responsible Party

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Prof. Marco Ferrari

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Department of Dental Materials and Fixed Prosthodontics of the University of Siena, Policlinico Le Scotte

Siena, Siena, Italy

Site Status

Countries

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Italy

Other Identifiers

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ABTM001

Identifier Type: -

Identifier Source: org_study_id

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