L-carnitine on the Prevention of Renal Scarring in Acute Pyelonephritis

Sponsor
Shahid Beheshti University (Other)
Overall Status
Unknown status
CT.gov ID
NCT02007889
Collaborator
(none)
78
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2
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Study Details

Study Description

Brief Summary

Risk factors for parenchymal damage in urinary tract infection are vesicoureteral reflux (VUR),obstructive uropathy,the number of flares of acute pyelonephritis(APN) and delay in treatment of acute infection.The pathogenesis of APN is related to bacterial virulenece,immune response,tissue factors,apoptosis and production of free radicals that lead to fibrosis and renal scarring. Oxidative stress in renal cells may be a critical factor in the pathogenesis of pyelonephritis whereas pharmacological management of the oxidative stress response may provide a therapeutic effect in preventing renal pathologies. Animal model show that L-carnitine alleviated oxidative stress, and acute renal inflammatory injury can be prevented much more effectively by carnitine in addition to conventional antibiotic treatment in pyelonephritis.This study is a simple randomized clinical trial (RCT) evaluating the effect of L-carnitine in addition to antibiotic on preventing renal scaring after acute pyelonephritis in children. Simple non- blind randomized clinical trial on 78 patients in 2 groups (intervention & control) is conducted.Children aged 1 month to 10 years with positive urine culture, clinical findings, and 99mTc-dimercaptosuccinic acid (DMSA) scintigraphy-based evidence in favor of acute pyelonephritis were enrolled into a clinical trial. Patients were excluded if they had neurogenic bladder, systemic hypertension, obstructive uropathy. Patients in Intervention group are administered 50 mg/kg/day carnitine in divided 2-3 times/day (maximum 3 g/day) in addition to antibiotic regimens and patients in control group received antibiotic regimens. Primary outcome is the development of renal scar by doing DMSA renal scan on the 7th day of admission and six months after the intervention and compared between groups and secondary outcome is the incidence and severity of pyelonephritis and response to treatment.

Condition or Disease Intervention/Treatment Phase
Phase 3

Study Design

Study Type:
Interventional
Anticipated Enrollment :
78 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
The Effect of L-carnitine on the Prevention of Renal Scarring in Children With Acute Pyelonephritis
Study Start Date :
Nov 1, 2013
Anticipated Primary Completion Date :
Aug 1, 2014
Anticipated Study Completion Date :
Oct 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: L-carnitine

50 mg/kg/day carnitine in divided 2-3 times/day (maximum 3 g/day) in addition to antibiotic regimens

Drug: L-carnitine
50 mg/kg/day carnitine in divided 2-3 times/day (maximum 3 g/day) in addition to antibiotic regimens

No Intervention: Control

control group received just antibiotic regimens without L-carnitine

Outcome Measures

Primary Outcome Measures

  1. Development of renal scar by doing DMSA renal scan [Seven and six months after the intervention]

Secondary Outcome Measures

  1. Severity of pyelonephritis and response to treatment. [Six month after intervention]

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Month to 10 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Children aged 1 month to 10 years with positive urine culture, clinical findings, and 99mTc-dimercaptosuccinic acid (DMSA) scintigraphy-based evidence in favor of acute pyelonephritis
Exclusion Criteria:
  • neurogenic bladder,

  • systemic hypertension,

  • obstructive uropathy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Isfahan University of Medical Sciences,Alzahra Hospital Isfahan Iran, Islamic Republic of 0098

Sponsors and Collaborators

  • Shahid Beheshti University

Investigators

  • Principal Investigator: Golnaz Vaseghi, Ph.D pharmacology, Physiology Research Center
  • Principal Investigator: Alaleh Gheisari, Pediatric Nephrologist,Isfahan University, Isfahan, Iran
  • Principal Investigator: Nahid Aslani, Resident of pediatrics, Isfahan University of Medical Sciences
  • Principal Investigator: Azadeh Eshraghi, Clinical Pharmacist, Shahid Beheshti University of Medical Sciences

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Azadeh Eshraghi, Clinical Pharmacist, Shahid Beheshti University
ClinicalTrials.gov Identifier:
NCT02007889
Other Study ID Numbers:
  • ShahidBU
First Posted:
Dec 11, 2013
Last Update Posted:
Dec 11, 2013
Last Verified:
Dec 1, 2013
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 11, 2013