To Study the Effect of Adjunctive Oral Methylprednisolone Therapy in Pediatric Urinary Tract Infection
Information source: National Cheng-Kung University Hospital
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Urinary Tract Infection
Intervention: Methylprednisolone (Drug)
Phase: Phase 3
Status: Not yet recruiting
Sponsored by: National Cheng-Kung University Hospital
Summary
Purposes of this study will be as follows:
1. To design a prospective, randomized, and open-labeled study to investigate the effect
and the side effect of MPD in combination with conventional antibiotics to affect
clinical course, outcome, and medical expenses.
2. To compare level of the urinary and serum cytokines before and after received MPD for
the following sub-aim:
I. To determine the population who is benefit from MPD to reduce the severity of clinical
course and subsequent renal scarring.
II. To understand the mechanism by which the MPD could shorten the clinical course and
reduce the renal scarring.
Clinical Details
Official title: To Study the Effect of Adjunctive Oral Methylprednisolone Therapy in Pediatric Urinary Tract Infection
Study design: Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: The proportion of patients with renal scar formation
Secondary outcome: Duration of the hospitalizationExpense of the hospitalization
Detailed description:
The urinary tract infection (UTI) is a common etiology of the febrile children and the acute
pyelonephritis (APN) happen in 70% children with the first febrile UTI. After the first APN,
the irreversible renal scarring takes place in about 40% patients. The sequela of the renal
scarring includes chronic kidney disease, hypertension, the complication during the
pregnancy, and even the end stage of renal diseases. Due to the progression of the
pathophysiology of the pyelonephritis and the renal scarring in the past years, we
understand that the inflammation is one of the important mechanisms. Therefore, there are
many animal studies clarifying the role of the anti-inflammation or antioxidant to reduce
the renal scarring. In our previous studies, Dr. Chiou Y. Y. and colleagues has provided the
evidence that the adjunctive methylprednisolone (MPD) can decrease the risk of the renal
scarring for patients with high risk APN, which was defined as inflammatory volume more than
4. 6 mL on technetium-99m-labeled dimercaptosuccinic acid scan or abnormal renal
ultrasonography results. Our study is the first human study demonstrating the solution for
the renal scarring. However, whether this result can be applied to the whole spectrum of the
UTI is still unknown. Purposes of this study will be as follows:
1. To design a prospective, randomized, and open-labeled study to investigate the effect
and the side effect of MPD in combination with conventional antibiotics to affect
clinical course, outcome, and medical expenses.
2. To compare level of the urinary and serum cytokines before and after received MPD for
the following sub-aim:
I. To determine the population who is benefit from MPD to reduce the severity of clinical
course and subsequent renal scarring.
II. To understand the mechanism by which the MPD could shorten the clinical course and
reduce the renal scarring.
According to these studies, we will provide a new and effective guideline to shorten disease
course, save medical expenses, and decrease the risk for renal scarring sequela.
Eligibility
Minimum age: N/A.
Maximum age: 16 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- 1week old ~ 16 years old children with UTI
Exclusion Criteria:
- Previous UTI
- Known GU tract obstruction
- Severe sepsis with vital signs change
- Antibiotics used
Locations and Contacts
Additional Information
Starting date: January 2015
Last updated: January 4, 2015
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