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Periodontal impact of anorexia nervosa and bulimia nervosa

Periodontal Impact of Eating Disorders: the PERIOED case-control study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN77400898
Enrollment
90
Registered
2016-11-16
Start date
2014-10-07
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

1. Anorexia nervosa 2. Bulimia nervosa Mental and Behavioural Disorders 1. Anorexia nervosa 2. Bulimia nervosa

Interventions

All participants attend one single visit at baseline. Firstly, this visit involves a patient interview in order to record the oral hygiene behaviors (dental visits frequency and tooth

Sponsors

Assistance Publique Hôpitaux de Paris (APHP)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Anorexia nervosa participants: 1. Age 18 to 65 years old 2. Female 3. A proper diagnosis of anorexia nervosa for at least 5 years 4. Affiliated to the French social insurance Bulimia nervosa participants: 1. Age 18 to 65 years old 2. Female 3. A proper diagnosis of bulimia nervosa for at least 5 years 4. Affiliated to the French social insurance Non-eating disorder participants: 1. Age 18 to 65 years old 2. Female 3. Non-eating disorder volunteer 4. Affiliated to the French social insurance

Exclusion criteria

Exclusion criteria: 1. Unable to speak French 2. Unable to read and/or understand the information form 3. Taking anti-inflammatory medications or antibiotics at dental examination 4. Previously received any dental treatment that could interfere with the periodontal status 3 months before the clinical examination (scaling and root planning, orthodontic treatment ongoing) 5. Having less than 10 teeth

Design outcomes

Primary

MeasureTime frame
Clinical Attachment Level (CAL) is calculated as follows: periodontal probing depth (in mm) added to gingival recession height (in mm), which are measured with a manual periodontal probe (6 sites per tooth) at the day of the oral examination.

Secondary

MeasureTime frame
Gingival inflammation is measured using the bleeding on probing score (% of sites) at the day of the oral examination.

Countries

France

Contacts

Public ContactHélène Rangé
helene.range@aphp.fr+33 6 1465 6947

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026