Growth of Infants Fed Hydrolysate Formulas

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)

Related Conditions & MeSH terms

Growth and Tolerance

See also
	Status	Clinical Trial	Phase
	Completed	`NCT04105686` - Growth and Tolerance of Young Infants Fed Infant Formula	N/A
	Completed	`NCT01808105` - Growth and Tolerance of Infants Fed Infant Formulas	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT04105686 - Growth and Tolerance of Young Infants Fed Infant Formula

N/A

Completed

NCT01808105 - Growth and Tolerance of Infants Fed Infant Formulas

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	NCT02006992
Study type	Interventional
Source	Abbott Nutrition
Contact
Status	Completed
Phase	N/A
Start date	March 2000
Completion date	November 2000

Growth of Infants Fed Hydrolysate Formulas

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms