Actively Recruiting

Age: 18Years - 40Years
All Genders
Healthy Volunteers
NCT07295197

Oral Indicators for ED Screening

Led by University of Bologna · Updated on 2025-12-19

461

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The main objective of this research project is to explore the capability of a standardized, evidence-based study tool (the OHEDs Checklist) in the early identification of oro-dental manifestations potentially indicative of an eating disorder. The secondary objective is to evaluate the sensitivity and specificity of the OHEDs Checklist in comparison with validated screening instruments for eating disorders, namely the ESP, SCOFF and DEQ questionnaires.

CONDITIONS

Official Title

Oral Indicators for ED Screening

Who Can Participate

Age: 18Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 40 years
  • Presence of at least 20 permanent teeth (third molars excluded)
  • Both males and females are eligible
  • Ability to provide written informed consent
Not Eligible

You will not qualify if you...

  • Pregnancy or breastfeeding
  • Use of systemic antibiotics within the previous month
  • Active orthodontic treatment
  • Presence of systemic diseases that may affect oral conditions, including diabetes, ulcerative colitis, Crohn's disease, Sj�f6gren's syndrome, HIV infection, hematologic diseases, neoplasms
  • Mental disorders or neuromotor deficits that may interfere with the oro-dental clinical signs evaluated by the OHEDs Checklist
  • Use of xerogenic medications or drugs that may alter salivary flow or oral/perioral mucosal conditions, including antihypertensives, beta-blockers, NSAIDs, antiparkinson medications, anxiolytics, antidepressants, neuroleptics

AI-Screening

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Trial Site Locations

Total: 1 location

1

Clinica Odontoiatrica - Reparto di Igiene Dentale, Università di Bologna

Bologna, Italy, 40125

Actively Recruiting

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Research Team

M

Marco Montevecchi

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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