The Effect of Renastart Formula Supplementation in Children With Acute Kidney Injury in Maintaining Normal Serum Electrolytes Levels - Trial NCT06218212
Access comprehensive clinical trial information for NCT06218212 through Pure Global AI's free database. This phase not specified trial is sponsored by Ain Shams University and is currently Completed. The study focuses on Acute Kidney Injury. Target enrollment is 24 participants.
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Study Focus
Sponsor & Location
Ain Shams University
Timeline & Enrollment
N/A
Feb 12, 2022
Jun 30, 2023
Primary Outcome
To evaluate the effectiveness and tolerability of Renastart formula in children with AKI and acute on top of CKD to correct and maintain normal serum levels of electrolytes.
Summary
This clinical trial will evaluate Renastart formula effectiveness in children with acute
 kidney injury (AKI) and acute on top of chronic kidney disease (CKD), in maintaining normal
 serum electrolytes levels without using electrolyte binders,24 patients will be recruited
 from Pediatric Nephrology Unit (PNU), Children's Hospital, Ain Shams University, they will be
 assigned randomly in to two arms, arm 1 including patients who will be treated by
 electrolytes binders, arm 2 including patients who will be treated by Renastart formula,
 after initial assessment serum electrolyte evaluation will be followed up monthly for 3
 months.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06218212
Non-Device Trial