Antibiotic Prophylaxis, Febrile Urinary Tract Infection, Voiding Cystourethrogram
Conditions
Brief summary
The current practice of pre-VCUG antibiotic prophylaxis is highly variable. A recent unpublished survey of Society of Fetal Urologists (SFU) completed by this study team found that 87% of respondents reported having patients who develop fUTI following VCUG, with 30% of respondents prophylaxing for fUTI in patients undergoing VCUG. The current lack of best practice guidelines regarding antibiotic prophylaxis prior to VCUG due to low quality of current literature, and a growing concern around risks of unnecessary antibiotic exposure suggests the need for an RCT. The results of this pilot trial will inform the ability to conduct a definitive RCT on this important subject. The results of the definitive trial would have important clinical and economic implications.
Detailed description
What are the Study Objectives? The primary objective of this pilot trial is to determine the feasibility of conducting a definitive trial investigating whether pre-VCUG antibiotic prophylaxis, when compared to placebo, decreases the risk of fUTI in infants undergoing VCUG for genitourinary abnormalities. The pilot trial will address specific feasibility outcomes including process, resources, management and scientific domains. The pilot will lay the groundwork for the eventual full trial. Funding for the full trial will be sought after preliminary data is collected from the pilot study. The primary objective for the definitive trial is to determine whether single-dose, preprocedural antibiotic prophylaxis compared to placebo lowers the risk of fUTI in children \< 3 years of age who are undergoing VCUG for the following indications: high-grade (SFU Classification III, IV/UTD 2,3) HN, ureteral dilatation, or bladder abnormalities found during renal ultrasound. The secondary outcomes of the definitive trial will include assessment of adverse event outcomes related to antibiotic prophylaxis administration, including antibiotic resistant UTI pathogens, episodes of antibiotic associated diarrhea, and C. difficile.
Interventions
DRUGAntibiotic Prophylaxis
This trial will contain two arms in which patients will be randomized to receive one dose of either Trimethoprim (if \< 2 months) or Trimethoprim-Sulfamethoxazole (if ≥ 2 months) or placebo in suspension. Dosing regimen for the active treatment (Trimethoprim) will be based on weight (5mg/kg of Trimethoprim component) with a maximum dosage of 320mg
OTHERPlacebo
The placebo group will receive an equal volume of placebo suspension that has been developed to have the same colour and taste as the antibiotic to preserve blinding.
Sponsors
Hamilton Health Sciences Corporation
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Masking description
Blinded
Intervention model description
This trial is a single center, parallel, blinded, randomized, placebo-controlled pilot trial in children
Eligibility
Sex/Gender
ALL
Age
No minimum to 3 Years
Healthy volunteers
Yes
Inclusion criteria
1. Children \<3 years of age undergoing VCUG for the following indications: high-grade SFU/UTD hydronephrosis, ureteral dilatation, or bladder abnormalities found during renal ultrasound 2. Parent or legal guardian able to provide informed consent
Exclusion criteria
1. Chronic antibiotic use 2. Allergy to Trimethoprim or Trimethoprim-Sulfamethoxazole
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Feasibility of pilot study: randomization, compliance, enrollment targets | 12 months | The primary feasibility outcomes for the pilot study will be recruitment rate (\>50% of eligible infants enrolled), randomization rate (percentage of participants randomized, \>95%), medication compliance rate (\>80%), percentage of the primary endpoints (febrile UTI) and cost of being in the trial per patient. We would also aim to demonstrate a \<15% rate of protocol violations, and loss to follow-up. The major clinical outcome for the pilot study is to determine the event rate of UTI in patient post-procedure to inform the sample size calculation for the larger trial. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Resource Allocation | 12 months | Secondary outcomes in the pilot study will be adequacy of research resource allocation, to understand if further study supports are required for the eventual multi-centre trial. Management outcomes include determining research coordinator capacity, processing times for each enrollment, and follow-up, time required for adjudication UTI events, and ensuring adequacy and accuracy of data management. We will also aim to understand potential barriers to recruitment, and compliance. Adverse events related to antibiotic use for patients will be recorded as well. |
| Febrile UTI within 7 days of VCUG Procedure | 7 days | Patients will be enrolled in the study for 7 days post VCUG, which is clinically considered the immediate post-procedure period. |
Contacts
Primary ContactSarah Khan, MD
Outcome results
None listed