The Impact of Material on Microbiota in Association With Tongue and Lip Piercing

NCT ID: NCT01039259

Last Updated: 2009-12-24

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

Total Enrollment

170 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-08-31

Study Completion Date

2009-02-28

Brief Summary

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Biofilms on oral piercings may serve as a bacterial reservoir and lead to systemic bacteraemia or local transmission of periopathogenic microbiota.

The investigators hypothesize that there are microbiological differences in bacterial samples collected from tongue /or lip piercings made of different materials. The investigators also hypothesize that the piercings carry the same characteristic bacteria as found in the piercing channels and that independently the biofilm on the tongue/adjacent teeth is similar to the other study locations.

85 subjects with tongue and 85 subjects with lip piercing will participate. Periodontal clinical parameters, traumata of hard tissues, and characteristics of the stud are evaluated. Sterile piercings of four different materials will be randomly allocated to the study subjects. After two weeks, microbiologic samples are collected and are processed by checkerboard DNA-DNA hybridization methods.

Detailed Description

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Conditions

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Bacteremia

Keywords

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adolescent body piercing/adverse effects tongue piercing tongue/microbiology

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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subjects with lip piercing

piercings of four different materials

Intervention Type DEVICE

randomly assigned sterile piercings are inserted for two weeks

subjects with tongue piercing

piercings of four different materials

Intervention Type DEVICE

randomly assigned sterile piercings are inserted for two weeks

Interventions

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piercings of four different materials

randomly assigned sterile piercings are inserted for two weeks

Intervention Type DEVICE

Other Intervention Names

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piercing materials: steel, titanium, polypropylene, polytetrafluoroethylene

Eligibility Criteria

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Inclusion Criteria

* lip/tongue piercing for at least six month in situ

Exclusion Criteria

* pregnancy and lactating women
* medication with known effects on gingival tissues
* antibiotic medication in the last six months or need for antibiotic prophylaxis
* chlorhexidine use in the last six months
* non-plaque induced gingival disease
* prior diagnosis of periodontitis
Minimum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Austrian Society of Periodontology

OTHER

Sponsor Role collaborator

Medical University Innsbruck

OTHER

Sponsor Role lead

Responsible Party

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Innsbruck Medical University

Principal Investigators

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Ines Kapferer, Dr.

Role: PRINCIPAL_INVESTIGATOR

Innsbruck Medical University

Locations

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Innsbruck Medical University

Innsbruck, , Austria

Site Status

Countries

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Austria

Other Identifiers

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AN3223 265/4.7

Identifier Type: -

Identifier Source: org_study_id