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Clinical Trial Summary

a single blinded randomized controlled clinical trial that was conducted to evaluate the role of zinc supplementation in improving the outcome of infants and children with sepsis in pediatric intensive care unit.


Clinical Trial Description

a single blinded randomized controlled clinical trial that was conducted to evaluate the role of zinc supplementation in improving the outcome of infants and children with sepsis in pediatric intensive care unit. The study included 72 cases that were randomly divided into 2 groups A- Group A (Zinc treated group): Included 36 cases who received oral zinc sulfate supplementation at doses ranging from 10 mg (infants) to 20 mg (under-five children) of elemental zinc per day, a dosage that is safe in these children. B- Group B: Included 36 cases who didn't receive zinc sulfate supplementation. Method of randomization: The cases were randomly divided into two groups using the closed envelope technique. The numbers from 1 to 72 were written in flat pieces of papers and put in closed envelopes that were randomly distributed to the participants. The cases with the odds number were allocated to the zinc treated group while the cases with the even numbers were allocated to the other group. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05366595
Study type Interventional
Source Mansoura University
Contact
Status Completed
Phase Phase 2
Start date July 31, 2019
Completion date August 1, 2022