Last updated: September 26, 2023
Sponsor: Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Overall Status: Active - Not Recruiting
Phase
3
Condition
Bladder Disorders
Enuresis
Birth Defects
Treatment
Cefixime
Amoxicillin-Potassium Clavulanate Combination
nitrofurantoin
Clinical Study ID
NCT02021006
PREDICT trial
Ages 1-4 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Age between 1 and 4 months (> 4 weeks and <20 weeks of post-natal age)
- Gestational age > 35 weeks
- Glomerular filtration rate (calculated according to Schwartz) > 15 ml/min/1.73 m2
- No previous symptomatic UTI
- Imaging Diagnostic work-up completed and presence of grade III to V vesicoureteralreflux
- Informed consent of parents
Exclusion
Exclusion Criteria:
- Age <1 and >4 months
- Gestational age < 35 weeks
- Glomerular filtration rate (calculated according to Schwartz) < 15 ml/min/1.73 m2 atthree months of age
- Patients with neurogenic bladder, myelomeningocele, ureteropelvic junction and/orureterovesical junction obstruction, or other malformations leading to potentialvoiding disturbances.
- Presence of urethral valves
- Patients with no or low grade reflux (grade I and II).
- Hypersensitivity to the all the utilized antimicrobial agent
- Children with serious clinical conditions which, according to the investigator,prevent them from being included in the study cohort.
- Use of experimental drugs in the month previous to the beginning of the study
- Children unable to follow the established protocol procedures or whose parents areunable to sign the informed consent.
Study Design
Total Participants: 292
Treatment Group(s): 5
Primary Treatment: Cefixime
Phase: 3
Study Start date:
December 01, 2013
Estimated Completion Date:
January 31, 2025
Study Description
Connect with a study center
Azienda Ospedaliera Universitaria di Bologna Policlinico S. Orsola Malpighi
Bologna, 40138
ItalySite Not Available
Pediatric Nephrology Dialysis and Transplant Unit IRCCS Ca'Granda
Milan, 20122
ItalySite Not Available
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