Randomized, double-blind, placebo-controlled clinical trial to evaluate the efficacy of an oral probiotic preparation in hidradenitis suppurativa treatment

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dc.date.accessioned2023-07-03T11:23:29Z
dc.date.available2023-07-03T11:23:29Z
dc.date.issued2023-04
dc.descriptionRandomized, double-blind, placebo-controlled clinical trial, to evaluate an oral probiotic effectiveness administered for 12 weeks on the hidradenitis suppurativa evolution. A total of 60 patients diagnosed with hidradenitis suppurativa will participate in the study, who will be randomized into two treatment groups in a 1:1 ratio (30 patients per group). The intervention groups are differentiated according to the treatment to be received: probiotic or placebo of similar appearance, along with standard therapy according to usual clinical practice. The 12 weeks of treatment are structured into three face-to-face visits: Visit 1 (initial; week 0), Visit 2 (intermediate; week 6) and Visit 3 (final; week 12).es
dc.description.abstractThe clinical trial has a randomized, double-blind, placebo-controlled design, which aims to evaluate the effect of an oral probiotic preparation administered for 12 weeks on the evolution of hidradenitis suppurativaes
dc.description.disciplineCiencias de la Alimentaciónes
dc.description.disciplineMedicinaes
dc.identifier.urihttp://hdl.handle.net/10952/6541
dc.language.isoenes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.accessRightsopen accesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectHidradenitis suppurativaes
dc.subjectAcne inversaes
dc.subjectOral probiotices
dc.subjectMicrobiotaes
dc.subjectMicrobiomees
dc.titleRandomized, double-blind, placebo-controlled clinical trial to evaluate the efficacy of an oral probiotic preparation in hidradenitis suppurativa treatmentes
dc.typeotheres
dspace.entity.typePublication

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