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Clinical effectiveness and bacteriological eradication of three different Short-COurse antibiotic regimens and single-dose fosfomycin for uncomplicated lower Urinary Tract infections in adult women (SCOUT study): study protocol for a randomised clinical trial

dc.contributor.authorGarcia-Sangenis, Ana
dc.contributor.authorMorros, Rosa
dc.contributor.authorAguilar-Sanchez, Mercedes
dc.contributor.authorMedina-Perucha, Laura
dc.contributor.authorLeiva Rus, Alfonso
dc.contributor.authorRipoll, Joana
dc.contributor.authorMartinez-Pecharroman, Mar
dc.contributor.authorBartolome-Moreno, Cruz B
dc.contributor.authorBotaya, Rosa Magallon
dc.contributor.authorMarin-Canada, Jaime
dc.contributor.authorMolero, Jose M
dc.contributor.authorMoragas, Ana
dc.contributor.authorTroncoso, Amelia
dc.contributor.authorMonfa, Ramon
dc.contributor.authorLlor, Carl
dc.contributor.authorSCOUT Study Group
dc.date.accessioned2024-09-18T06:42:03Z
dc.date.available2024-09-18T06:42:03Z
dc.date.issued2021-11
dc.description.abstractIntroduction: Uncomplicated lower urinary tract infections (uLUTI) are a common problem in primary care. Current local guidelines recommend the use of a single 3 g dose of fosfomycin. However, most general practitioners (GP) prefer short-course therapies to single-dose therapy. No study has compared head-to-head short-course antimicrobial agents for uLUTIs. Therefore, the aim of this randomised clinical trial is to compare three different short-course antibiotic therapies with a single-dose of fosfomycin for these infections. Methods and analysis This will be a pragmatic, multicentre, parallel group, open trial. Women aged 18 or older and with symptoms of uLUTI and a positive urine dipstick analysis will be randomised to one of the following four groups: a single dose of 3 g of fosfomycin, 2 days of 3 g of fosfomycin o.d., 3 days of pivmecillinam 400 mg three times per day (t.i.d) or 5 days of nitrofurantoin 100 mg t.i.d. A total sample of 1120 patients was calculated. The primary endpoint is clinical effectiveness at day 7, defined as cure of symptoms reported by the patients in a diary including four symptoms: dysuria, urgency, frequency and suprapubic pain, which will be scored on a 4-point severity scale (not present/mild/moderate/severe). Follow-up visits are scheduled at days 7 (phone call), 14 and 28 for assessing evolution. Urine samples will be collected in the three on-site visits and urine cultures performed. If positive, antibiograms for the three antibiotics studied will be performed. Bacterial eradication will be measured at days 14 and 28. Ethics and dissemination The study was approved by the Ethical Board of IDIAP Jordi Gol (reference number: 21/173-AC) and Spanish Agency of Medicines and Medical Devices. The findings of this trial will be disseminated through research conferences and peer-review journals.en
dc.description.sponsorshipThe SCOUT Study received a research grant from the Carlos III Institute of Health (ISCIII), Ministry of Science and Innovation (Spain), awarded in the 2020 call under the Academic Clinical Trials Call, with reference ICI20/00100, by Primary Care Prevention and Heath Promotion Network GRenSSAP (code RD16/0007/0001), Balearic Islands (code RD16/0007/0008), Aragon (code RD16/0007/0005), Madrid (code RD16/0007/0013) and by European Union ERDF funds (European Regional Development Fund).es_ES
dc.format.number11es_ES
dc.format.pagee055898es_ES
dc.format.volume11es_ES
dc.identifier.citationGarcia-Sangenis A, Morros R, Aguilar-Sanchez M, Medina-Perucha L, Leiva A, Ripoll J, et al. Clinical effectiveness and bacteriological eradication of three different Short-COurse antibiotic regimens and single-dose fosfomycin for uncomplicated lower Urinary Tract infections in adult women (SCOUT study): study protocol for a randomised clinical trial. BMJ Open. 2021 Nov;11(11):e055898.en
dc.identifier.doi10.1136/bmjopen-2021-055898
dc.identifier.issn2044-6055
dc.identifier.journalBMJ Openes_ES
dc.identifier.otherhttps://hdl.handle.net/20.500.13003/19496
dc.identifier.pubmedID34824124es_ES
dc.identifier.puiL636536246
dc.identifier.scopus2-s2.0-85120624436
dc.identifier.urihttps://hdl.handle.net/20.500.12105/23156
dc.identifier.wos724352600029
dc.language.isoengen
dc.publisherBMJ Publishing Group
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/ICI20/00100en
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD16/0007/0001en
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD16/0007/0008en
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD16/0007/0005en
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD16/0007/0013en
dc.relation.publisherversionhttps://dx.doi.org/10.1136/bmjopen-2021-055898en
dc.rights.accessRightsopen accessen
dc.rights.licenseAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectMicrobiology
dc.subjectPrimary care
dc.subjectPublic health
dc.subjectUrinary tract infections
dc.subject.decsResultado del Tratamiento*
dc.subject.decsInfecciones Urinarias*
dc.subject.decsHumanos*
dc.subject.decsDistribución Aleatoria*
dc.subject.decsFosfomicina*
dc.subject.decsEnsayos Clínicos como Asunto*
dc.subject.decsFemenino*
dc.subject.decsAdulto*
dc.subject.decsNitrofurantoína*
dc.subject.decsAntibacterianos*
dc.subject.meshRandom Allocation*
dc.subject.meshClinical Trials as Topic*
dc.subject.meshNitrofurantoin*
dc.subject.meshAdult*
dc.subject.meshAnti-Bacterial Agents*
dc.subject.meshFemale*
dc.subject.meshFosfomycin*
dc.subject.meshTreatment Outcome*
dc.subject.meshUrinary Tract Infections*
dc.subject.meshHumans*
dc.titleClinical effectiveness and bacteriological eradication of three different Short-COurse antibiotic regimens and single-dose fosfomycin for uncomplicated lower Urinary Tract infections in adult women (SCOUT study): study protocol for a randomised clinical trialen
dc.typeresearch articleen
dspace.entity.typePublication
relation.isPublisherOfPublication7ffe3d60-d8d6-4023-8234-aa60d8420845
relation.isPublisherOfPublication.latestForDiscovery7ffe3d60-d8d6-4023-8234-aa60d8420845

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