CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 717 enrolled
Drug / intervention
Cefixime +3 moredrug
Likely dose
Cefixime 8 mg/kgfrom record
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Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01595529
NCT01595529Phase 2Completed

Targeted Clinical Trials to Reduce the Risk of Antimicrobial Resistance The SCOUT Study: "Short Course Therapy for Urinary Tract Infections in Children"

National Institute of Allergy and Infectious Diseases (NIAID)·interventional·Posted May 10, 2012·Updated Aug 6, 2020

In Brief

A Phase 2 clinical trial evaluating Cefixime, Cephalexin, and 2 other interventions for Urinary Tract Infection. Completed, enrolled 717 participants across 1 site.

Detailed Summary

The SCOUT study is a multi-center, centrally randomized, double-blind, placebo-controlled non-inferiority clinical trial. 746 participants will be enrolled over a 4.5 year period. 672 will be evaluated for the study's primary outcome measure. After the first 5 days of primary care physician initiated antimicrobial therapy, patients who are afebrile and asymptomatic will then be randomized (1:1) to the standard course therapy arm of 5 more days of the same antibiotic therapy or the short course therapy arm of a placebo for 5 more days (for 10 days total). The primary objective of this study is to determine if halting antimicrobial therapy in subjects who have exhibited clinical improvement 5 days after starting antibiotic therapy (short course therapy) have the same failure rate (symptomatic UTI) through visit Day 11-14 as subjects who continue to take antibiotics for an additional 5 days (standard course therapy).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedMay 10, 2012
Enrollment StartMay 18, 2012
Primary CompletionJun 30, 2019
Study CompletionAug 12, 2019
TodayJul 2, 2026
Enrollment to primary: 7.1 yearsPosted 14.1 years ago

Interventions

Cefiximedrug

Cefixime 8 mg/kg/day orally, in 1 dose, with a maximum of 400 mg. Subjects originally receiving Cefdinir will receive Cefixime.

Cephalexindrug

Cephalexin 50mg/kg/day in 3 divided doses

Placeboother

Placebo to match the other four active treatments

Trimethoprim/Sulfamethoxazoledrug

8 mg/kg/day of Trimethoprim-sulfamethoxazole (TMP-SMX) orally in 2 divided doses, with a maximum dose of 160 mg twice a day.