A2 GUM Post-Market Effectiveness Study

Clinical Trial Description

This post-market study primarily aims to assess the real-life effectiveness of a newly-launched A2 milk on toddlers' gut comfort via evaluating individual GI symptoms and GI-related behaviors compared with other milk products and milk alternatives. ;

Study Design

Related Conditions & MeSH terms

Protein Intolerance

See also
Status	Clinical Trial	Phase
Completed	`NCT04771377` - Effect of Protein Supplementation and a Structured Exercise Program on Muscle in Women After Bariatric Surgery.	N/A
Completed	`NCT03884309` - Evaluation of Infants Fed an Extensively Hydrolyzed Infant Formula	N/A
Recruiting	`NCT04615858` - Genepro Generation 3 Protein Bioavailability Compared to Whey Protein	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT04771377 - Effect of Protein Supplementation and a Structured Exercise Program on Muscle in Women After Bariatric Surgery.

N/A

Completed

NCT03884309 - Evaluation of Infants Fed an Extensively Hydrolyzed Infant Formula

N/A

Recruiting

NCT04615858 - Genepro Generation 3 Protein Bioavailability Compared to Whey Protein

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	NCT03698058
Study type	Interventional
Source	Nestlé
Contact
Status	Completed
Phase	N/A
Start date	September 15, 2018
Completion date	March 31, 2019

A2 GUM Post-Market Effectiveness Study

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms