Nutritive Effects of a Cow's Milk Based Formula Fed to Young Children

Clinical Trial Description

This study aims to determine if a cow's milk-based formula with added nutrients has an effect on memory, reaction time, strategy or other cognitive development indicators in children 4-5 years of age. ;

Study Design

See also
Status	Clinical Trial	Phase
Terminated	`NCT04413604` - Micronutrient Status in Children Aged 1-3 Years Consuming Their Habitual Diet With or Without Young Children's Milk	N/A
Completed	`NCT05440604` - Nutrient and Immunity Status in Children Aged 3-5 Years Consuming Their Habitual Diet With or Without Fortified Milk	N/A
Recruiting	`NCT05798494` - PRE-Pregnancy Weight Loss And the Reducing Effect on CHILDhood Overweight - Aarhus	N/A

See also

Status

Clinical Trial

Phase

Terminated

NCT04413604 - Micronutrient Status in Children Aged 1-3 Years Consuming Their Habitual Diet With or Without Young Children's Milk

N/A

Completed

NCT05440604 - Nutrient and Immunity Status in Children Aged 3-5 Years Consuming Their Habitual Diet With or Without Fortified Milk

N/A

Recruiting

NCT05798494 - PRE-Pregnancy Weight Loss And the Reducing Effect on CHILDhood Overweight - Aarhus

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT02776592
Study type	Interventional
Source	Mead Johnson Nutrition
Contact
Status	Completed
Phase	N/A
Start date	July 20, 2016
Completion date	December 23, 2016

Nutritive Effects of a Cow's Milk Based Formula Fed to Young Children

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms