Other Clinical Trial - Pilot Study in the Cholesterol Absorption Reduction

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject)

Related Conditions & MeSH terms

Hypercholesterolemia
Mildly Hypercholesterolemic Subjects

See also
Status	Clinical Trial	Phase
Completed	`NCT01574469` - Effect of the Consumption of a Fermented Milk Enriched With Plant Sterols (France)	N/A
Completed	`NCT01571882` - Effects of Fermented Milk Product Enriched With Plant Sterols and Policosanols in Mild Hypercholesterolaemic Adults	N/A
Completed	`NCT01574482` - Effect of the Consumption of a Fermented Milk Enriched With Plant Sterols (Italy)	N/A
Completed	`NCT02376660` - Effect of Oats on Lipid Profile	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT01574469 - Effect of the Consumption of a Fermented Milk Enriched With Plant Sterols (France)

N/A

Completed

NCT01571882 - Effects of Fermented Milk Product Enriched With Plant Sterols and Policosanols in Mild Hypercholesterolaemic Adults

N/A

Completed

NCT01574482 - Effect of the Consumption of a Fermented Milk Enriched With Plant Sterols (Italy)

N/A

Completed

NCT02376660 - Effect of Oats on Lipid Profile

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	NCT01571869
Study type	Interventional
Source	Danone Research
Contact
Status	Completed
Phase	N/A
Start date	April 2005
Completion date	April 2006

Pilot Study in the Cholesterol Absorption Reduction After Consumption of Low-fat, Drinkable Fermented Milk Enriched With Plant Sterols

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms