Oral Formulation of Insulin for Preterm Infants

Status Terminated

Clinical Trial Summary

The study will evaluate the effect of oral formulation of insulin on preterm infants, born between 26-33 weeks of pregnancy, weighing over 750 grams, who meet the inclusion and exclusion criteria established in this protocol.

Clinical Trial Description

The study will aim to determine whether an oral formulation of insulin administration enhances gastrointestinal maturation. The gastrointestinal maturation will be evaluated by the ability of premature infants to achieve complete enteral feeds. The insulin concentration administered in the study is physiological and within the insulin concentration range present in human breast milk and colostrum. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01093638
Study type	Interventional
Source	Elgan Pharma Ltd.
Contact
Status	Terminated
Phase	Phase 2
Start date	August 2010
Completion date	January 2016

View Details

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