NCT02670863

Safety and Efficacy Study

Safety and Efficacy of a New Term Infant Formula Supplemented With A Prebiotic: a Doubleblind, Randomized, Controlled Trial

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 239 (actual)
• Sponsor: Société des Produits Nestlé (SPN) · Industry
• Sex: All
• Age: 21 Days – 26 Days
• Healthy volunteers: Accepted

Summary

The purpose of this study is to evaluate the safety and efficacy of the experimental formula supplemented with a prebiotic vs the control formula.

Detailed description

Randomized, double-blind, controlled interventional clinical trial design. The purpose of this study is to evaluate the safety and efficacy of a new term infant formula supplemented with a prebiotic vs a standard infant formula fed for 150 days to healthy, term infants.

Conditions

• Infant Term Birth

Interventions

Type	Name	Description
OTHER	Experimental Infant Formula	Standard bovine milk-based term infant formula supplemented with a prebiotic, fed ad libitum
OTHER	Standard Infant Formula	Standard bovine milk-based term infant formula, fed ad libitum

Timeline

• Start date: 2016-01-21
• Primary completion: 2017-03-01
• Completion: 2017-05-01
• First posted: 2016-02-02
• Last updated: 2021-10-11

Locations

1 site across 1 country: Philippines