Periodontal Impact of Eating Disorders (the PERIOED Study)

NCT ID: NCT02960152

Last Updated: 2017-05-02

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

UNKNOWN

Total Enrollment

90 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-10-31

Study Completion Date

2018-01-31

Brief Summary

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This study evaluated the periodontal status of patients suffering from eating disorders (anorexia nervosa and bulimia nervosa). The work hypothesis is that eating disorder patients have a higher risk for periodontal diseases than non-eating disorder subjects.

Detailed Description

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Eating disorders have been associated with poor oral health. However, the relationship between eating disorders and periodontal diseases is less-established. Participants will be periodontally assessed using a full-mouth clinical evaluation.

Conditions

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Periodontal Diseases Eating Disorder Anorexia Nervosa Bulimia Nervosa

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Anorexia Nervosa

interview and periodontal full-mouth examination

diagnostic

Intervention Type OTHER

full-mouth periodontal examination

Bulimia Nervosa

interview and periodontal full-mouth examination

diagnostic

Intervention Type OTHER

full-mouth periodontal examination

Control

interview and periodontal full-mouth examination

diagnostic

Intervention Type OTHER

full-mouth periodontal examination

Interventions

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diagnostic

full-mouth periodontal examination

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* In and out eating disorder patients
* Subject with a diagnosis of anorexia nervosa or bulimia nervosa for at least 5 years
* Subject affiliated to the French social insurance

Exclusion Criteria

* Subject who do not speak French
* Subject who is not able to read and/or understand the information form
* Subject who take anti-inflammatory medications or antibiotics at dental examination
* Subject who has received any dental treatment that could interfere with the periodontal status 3 month before the clinical examination (scaling and root planning, orthodontic treatment ongoing)
* Subject who has less than 10 teeth
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role collaborator

University Paris 7 - Denis Diderot

OTHER

Sponsor Role lead

Responsible Party

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Hélène Rangé

Dr

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Philippe Bouchard, DDS, PhD

Role: STUDY_CHAIR

Paris Diderot University

Locations

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Rothschild Hospital

Paris, , France

Site Status RECRUITING

Paul Brousse Hospital

Villejuif, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Hélène Rangé, DDS, PhD

Role: CONTACT

33 6 23 98 02 59

Facility Contacts

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Hélène Rangé, DDS, PhD

Role: primary

33 6 23 98 02 59

Damien Ringuenet, MD

Role: primary

33 1 45 59 33 71

Other Identifiers

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13588

Identifier Type: -

Identifier Source: org_study_id

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