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Clinical Trial Summary

The objective of this study is to compare the post-discharge growth of preterm infants fed with 2 different post discharge formulas.


Clinical Trial Description

Infants will be randomized upon discharge from the NICU. We will follow weight, height and head circumference for three months following discharge, In addition any feeding difficulties will be noted. ;


Study Design

Endpoint Classification: Bio-equivalence Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT01759134
Study type Interventional
Source Shaare Zedek Medical Center
Contact
Status Terminated
Phase Phase 4
Start date January 2013
Completion date June 2014

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