Compuls-BED-Severity

Recruiting Observational Study
Binge-Eating Disorder
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 65
Sex
Any
Study type
Observational
Participants needed
200 (estimated)
Sponsor
Laval University · Other
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About This Trial
* Binge Eating Disorder (BED) has been fairly recently introduced into the Diagnostic and Statistical Manual 5 psychiatric classification and its severity criteria are still not well established. * Moreover, it remains unclear whether BED is associated with greater metabolic severity or more somatic comorbidities, especially in obesity. * Improved BED severity staging could lead to a better defini…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * men or women aged 1 * participants eligible for bariatric surgery (BMI\>40, or BMI\>35 with severe comorbidities) * participants scheduled for medical evaluation and treatment of obesity at the IUCPQ Obesity Clinic (BMI≥30) * participants scheduled for evaluation and treatment…
Contacts

Sylvain Iceta, MD, PhD

+1 (418) 656-8711

equipe.iceta@criucpq.ulaval.ca

CONTACT

Pelletier Melissa

+1 (418) 656-8711

equipe.iceta@criucpq.ulaval.ca

CONTACT