No Interventional study
Otherno interventional study
Recruiting
NCT Number: NCT04352036
Constitution of a Prospective Cohort of Patients With Acute Suppurative Hidrosadenitis Followed in the Great West: the COVER Cohort (Verneuil Cohort)
Our primary objective with this cohort will be to define the different phenotypes of acute hidrosadenitis, the characterization of which is essential to define suitable therapeutic approaches. Indeed, our recent data allow us to note that there would be different phenotypes of acute hidrosadenitis and therefore different pathologies inducing different follow-ups and care.
Recruiting
Interested in participating?
Request InfoKey information
Conditions
Sex eligibility
All sexes
Study type
Observational
Primary location
CHU Angers, Angers, France
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Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patient diagnosed with acute hidrosadenitis by a dermatologist
- Patient agreeing to be part of the study
Exclusion criteria
- Major under guardianship
- Protected persons
Treatment and study plan
Primary outcomes
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Description of the natural history and identification of the different clinical forms of acute hidrosadenitis
Time frame: through study completion, an average of 3 years
history of the disease, classification of Hurley, Canoui-Poitrine and van der Zee and Jemec
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Prevalence of severe forms (grade II, III)
Time frame: through study completion, an average of 3 years
Number of patients with severe disease (grades II and III)
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Definition of different phenotypes of acute hidrosadenitis
Time frame: through study completion, an average of 3 years
patient history, Canoui-Poitrine and van der Zee and Jemec classification, blood and urine tests, imaging
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Identify the environmental factors associated with the chronicity of the disease
Time frame: through study completion, an average of 3 years
socio-demographic data
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Identify the environmental factors associated with the chronicity of the disease
Time frame: through study completion, an average of 3 years
questionnaire for collecting dietary habits
-
Identify the environmental factors associated with the chronicity of the disease
Time frame: through study completion, an average of 3 years
biological nutritional assessment research for a dysmetabolic syndrome
-
Identify the environmental factors associated with the chronicity of the disease
Time frame: through study completion, an average of 3 years
research for a dysmetabolic syndrome
-
Identify the environmental factors associated with the chronicity of the disease
Time frame: through study completion, an average of 3 years
lifestyle questionnaire assessing the impact on quality of life
Study contacts
Contact information is provided by the study sponsor or research team.
Sponsors and collaborators
Lead sponsor
Nantes University Hospital
Other
Registry information
Acronym: COVER
Important dates
- Study start
- 2022
- Primary completion
- 2030
- Study completion
- 2030
- First posted
- Apr 17, 2020
- Registry last updated
- Sep 5, 2025
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.