Identifier to cite or link to this item: https://hdl.handle.net/20.500.13003/18701
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
Identifiers
eISSN: 2044-6055
WOS ID: 000724352600029
Scopus EID: 2-s2.0-85120624436
PMID: 34824124
Embase PUI: L636536246
Share
Statistics
Item usage statisticsMetadata
Show Dublin Core item recordAuthor
Garcia-Sangenís, Ana; Morros, Rosa; Aguilar-Sánchez, Mercedes; Medina-Perucha, Laura; Leiva Rus, Alfonso



Publication date
2021-11-25Document type
research articleCitation
Garcia-Sangenís A, Morros R, Aguilar-Sánchez 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 t. BMJ Open. 2021 Nov 25;11(11):e055898.Abstract
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.
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.
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.
NCT04959331; EudraCT Number: 2021-001332-26.
January 2022 to April 2023.
Publisher version
https://doi.org/10.1136/bmjopen-2021-055898MeSH
Random AllocationClinical Trials as Topic
Nitrofurantoin
Adult
Anti-Bacterial Agents
Female
Fosfomycin
Urinary Tract Infections
Treatment Outcome
Humans
DeCS
Infecciones UrinariasResultado del Tratamiento
Humanos
Distribución Aleatoria
Fosfomicina
Ensayos Clínicos como Asunto
Femenino
Adulto
Nitrofurantoína
Antibacterianos
This item appears in following Docusalut collections
Atención Primaria de Mallorca - APMALL > Comunicación científicaInstituto de Investigación Sanitaria Islas Baleares - IDISBA > Comunicación científica