Effect of Escalating Doses of a Novel Viscous Polysaccharide on

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Prevention

See also
Status	Clinical Trial	Phase
Completed	`NCT01580150` - Effects of Berries on Post-meal Blood Sugar	N/A
Completed	`NCT00935350` - Reduction of the Glycemic Index by a Novel Viscous Polysaccharide	Phase 2/Phase 3
Completed	`NCT01108328` - Evaluation of Subjective Ratings of Appetite and Glucoregulation of a Low Calorie Diet Supplemented With a High Viscosity Polysaccharide (PolyGlycopleX - PGX)	Phase 3

See also

Status

Clinical Trial

Phase

Completed

NCT01580150 - Effects of Berries on Post-meal Blood Sugar

N/A

Completed

NCT00935350 - Reduction of the Glycemic Index by a Novel Viscous Polysaccharide

Phase 2/Phase 3

Completed

NCT01108328 - Evaluation of Subjective Ratings of Appetite and Glucoregulation of a Low Calorie Diet Supplemented With a High Viscosity Polysaccharide (PolyGlycopleX - PGX)

Phase 3

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	NCT00801814
Study type	Interventional
Source	Glycemic Index Laboratories, Inc
Contact
Status	Completed
Phase	Phase 2/Phase 3
Start date	April 2006
Completion date	August 2006

Effect of Escalating Doses of a Novel Viscous Polysaccharide on Postprandial Glycemia

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms