Immediate Implant Placement in the Molar Regions

NCT ID: NCT00226148

Last Updated: 2009-09-10

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

EARLY_PHASE1

Total Enrollment

92 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-09-30

Study Completion Date

2009-09-30

Brief Summary

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The purpose of this study is to look at the bonehealing when a molar has been extracted and immediately replaced by an implant leaving some defects around the implant.

The defects are being treated in three different with the hypothesis that the three ways of treatment result in equal bonehealing.

Detailed Description

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This study is a randomized clinically controlled study with three group of each thirty patients, where the bonehealing after immediate implantplacement in molarregions is being investigated.

Totally 90 patients are going to get a molar tooth extracted and immediately replaced with an implant (Brånemark System, Wide Platform). The molar tooth should be in such a condition that is has to be extracted.

Extracting a molar leaves a defect which cannot completely be filled out by an implant. The 90 patients are therefore randomised into 3 groups according to how the perimarginal bonedefects around the placed implants are being treated: 1. Bonechips 2. Membrane 3. Bonechips+Membrane. The bonehealing of the defects around the implants are then compared the groups in between. The amount of newly formed bone is being estimated too by digital radiography and subtractionradiography. Furthermore the prognosis for immediate placed implants in molar regions in relation to the method of defectreconstruction one year after crown delivery is also being investigated. All the investigations are conducted with the Ho-hypothesis that there is no difference in the bonehealing the three groups in between.

Conditions

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Periodontitis Dental Caries Periapical Periodontitis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Use of a membrane to cover bonedefects around implant

Intervention Type PROCEDURE

Use of bonechips to fill up defects around implant

Intervention Type DEVICE

Use of membrane and bonechips to manage defects

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* A molar tooth which has to be extracted
* Healthy persons with only mild systemic disease with no functional limitation

Exclusion Criteria

* Pregnant
* Any disease that is influencing the turnover of bone or oral mucosa
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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The Danish Medical Research Council

OTHER

Sponsor Role collaborator

University of Aarhus

OTHER

Sponsor Role lead

Responsible Party

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Dental School, Aarhus University

Principal Investigators

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Ann Wenzel, Prof.Dr.Odont, Ph.d.,DDS

Role: STUDY_CHAIR

The Royal Dental College of Aarhus

Locations

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The Royal Dental College of Aarhus

Aarhus, Aarhus, Denmark

Site Status

Countries

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Denmark

References

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Urban T, Kostopoulos L, Wenzel A. Immediate implant placement in molar regions: a 12-month prospective, randomized follow-up study. Clin Oral Implants Res. 2012 Dec;23(12):1389-97. doi: 10.1111/j.1600-0501.2011.02319.x. Epub 2011 Nov 25.

Reference Type DERIVED
PMID: 22117841 (View on PubMed)

Other Identifiers

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22-04-0281

Identifier Type: -

Identifier Source: secondary_id

2005/0091

Identifier Type: -

Identifier Source: org_study_id

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