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The study evaluates the efficacy of an adapted antibiotherapy in Hurley stage 2 active Hidradenitis Suppurativa patients versus tetracycline derivative
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Lead Sponsor
Institut Pasteur
Collaborators
NCT06958211 · Hidradenitis Suppurativa
NCT06921850 · Hidradenitis Suppurativa
NCT05889182 · Hidradenitis Suppurativa
NCT05243966 · Abdominal Wound Dehiscence, Necrotizing Soft Tissue Infection, and more
NCT06993233 · Hidradenitis Suppurativa (HS)
Hôpital de la Timone
Marseille
Centre Médical de l'Institut Pasteur
Paris
Hopital St Joseph
Paris
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Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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