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7-day Compared With 10-day Antibiotic Treatment for Febrile Urinary Tract Infections in Children

7-day Compared With 10-day Antibiotic Treatment for Febrile Urinary Tract Infections in Children: a Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03221504
Enrollment
221
Registered
2017-07-18
Start date
2018-01-01
Completion date
2020-01-31
Last updated
2018-03-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urinary Tract Infections in Children

Keywords

urinary tract infections, pyelonephritis, cefuroxime, children

Brief summary

The investigators aim to assess the effectiveness of a 7-day compared with a 10-day course of antibiotic treatment for febrile urinary tract infections (UTIs) in children. It is formulated a hypothesis that a 7-day course of antibiotic therapy is equally effective as a 10-day course of therapy and would entail a lower risk of adverse events and better compliance.

Detailed description

In previously published European and global guidelines, there has been no consensus among experts regarding the duration of therapy for a febrile UTI. Depending on the recommendation, the duration of treatment should be between 7-14 days. 221 patients aged 3 months to 7 years with febrile UTIs (defined as a combination of fever and leukocyturia in urine sediment) will be randomly assigned to receive a 7-day treatment arm (7 days of cefuroxime/cefuroxime axetil followed by 3 days of blinded placebo) or a 10-day treatment arm (7 days of cefuroxime/cefuroxime axetil followed by 3 days of blinded cefuroxime axetil). The primary outcome measure will be frequencies of recurrence and reinfection of UTI during the 6 months after the intervention. The secondary outcome measures will be antibiotic-associated diarrhea and compliance.

Interventions

Patients will receive cefuroxime axetil orally. Treatment will involve the supply of cefuroxime axetil 30 mg/kg/d in two divided doses (in blinded bottles).

Patients will receive placebo orally (in blinded bottles). The volume of the placebo will be like cefuroxime syrup.

Sponsors

Medical University of Warsaw
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
3 Months to 7 Years
Healthy volunteers
No

Inclusion criteria

(must have all): * children aged from 3 months to 7 years * clinical diagnosis of a febrile UTI at presentation according to urinalysis (white blood cells in the sediment \>10 in the field of view); * fever ≥38°C * positive urine collection with sensitivity for cefuroxime * treatment cefuroxime or cefuroxime axetil for 7 days

Exclusion criteria

(must have one): * history of a UTI in the last 3 months * prophylaxis for UTI * antibiotic therapy in the last month * known allergy to the study drugs * immunosuppression therapy * disease with immune deficiency * children with other coexisting infection, e.g. meningitis, sepsis, pneumonia, otitis * severe obstructive uropathy

Design outcomes

Primary

MeasureTime frameDescription
frequencies of recurrence of UTI3 months after interventionNew onset of symptomatic UTI within the 3 months follow-up period. The recurrence of a UTI is diagnosed when the next infection is caused by the same microorganism during 3 months following the treatment of a UTI.

Secondary

MeasureTime frameDescription
frequencies of reinfection of UTI6 months after interventionThe reinfection of a UTI is diagnosed when the next infection is caused by a different bacteria.
antibiotic-associated diarrhoea (AAD), compliance7 days after interventionAAD is defined by the daily production of at least 3 loose or watery stools for at least 48 hours during antibiotic treatment and 7 days after administration of the antibiotic. Compliance with the study protocol will be assessed by direct interview with the patient and/or caregiver and by measuring the amount of the fluid left in the bottle at the end of the intervention.

Countries

Poland

Contacts

Primary ContactMaria Daniel, MD
maria.daniel@wum.edu.pl+48696477117

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026