Comparison of Psyllium and Microcrystalline Cellulose on Glycemic Measures in Subjects With Impaired Fasting Glucose

Completed · Not applicable

Conditions studied: Impaired Fasting Glucose

In brief

The Purpose of this study is to compare the effects of 2 types of dietary fiber, psyllium and microcrystalline cellulose (MCC), on glycemic measures in subjects with impaired fasting glucose.

Key facts

Study ID

NCT01549600

Run by

Procter and Gamble

People needed

18

Starts

2012-02-01

Expected to finish

2013-05-01

Last updated by the study team

2014-10-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• be male or female,
• at least 18 years of age
• in generally good health for the pre-type 2 diabetes population;
• if female, be postmenopausal or if of child-bearing capacity agree to use an adequate form of contraception
• have not used any psyllium containing products within the past 3 months;
• be willing to refrain from taking any psyllium containing products during the study;
• be willing to maintain a lifestyle habits for the duration of the study;
• have a fasting serum glucose of 110 - 125 mg/dL

You may not qualify if…

• if female, are pregnant or nursing (lactating);
• have a history of diabetes (diagnosis) or is currently taking medications for diabetes
• participated in a clinical drug study or used investigational drug during the previous 30 days;
• have symptoms and signs suggestive of significant underlying disease, or acute onset of new symptoms and signs of major organ disease, that could become unstable during the trial requiring urgent medical intervention
• have evidence of or treatment history of malignancy within the previous 5 years;
• currently alcohol dependent;
• used anti-psychotics in the previous 3 months;
• used systemic steroidal agents within the last 30 days;
• had used oral or systemic antibiotics or any over-the-counter (OTC) bactericidal medication (eg, bismuth salts) within the last 30 days;
• has been taking any medication that may affect blood glucose or GI motility (eg, calcium channel blockers, beta blockers, antimuscarinics, salicylates etc.) for less than 30 days or 5 times the half life of the drug (need to be stable on the medication);
• have evidence of immunodeficiency including subjects currently taking systemic corticosteroids or immunosuppressive drugs
• have a major psychiatric disorder, including major depression, psychoses, alcohol or substance abuse within the past 2 years;
• has a known sensitivity or allergy to any components of study products, including psyllium and aspartame (see Section 3.5.3);
• were previously screened (ie, Visit 1 procedures) for participation in this study and failed to meet entry criteria;
• have difficulty swallowing

Where it is running

• Duke University Medical Center — Durham, North Carolina, United States

Full record on ClinicalTrials.gov

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