Expired Study
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Miami, Florida 33161


Purpose:

To compare the glucose response in tube fed subjects with type 2 diabetes of a standard enteral product to that of a diabetes-specific enteral product


Criteria:

Inclusion Criteria: - signed and dated informed consent - diagnosis of type 2 diabetes - HbA1c between 7.0 and 9.0% - 18 - 75 years of age - currently receiving a standard enteral product - anticipated duration on tube feeding at least one month - 100% of patient's nutrient and energy needs are anticipated to be met by enteral nutrition support - anticipated life expectancy is more than or equal to 6 months - free of infections - no change in medications within 2 weeks prior to screening that could profoundly affect blood glucose Exclusion Criteria: - composition of either product is inappropriate for the patient due to allergies or intolerance to any ingredient found in the study products - composition of either product is inappropriate for the patient due to protein, fluid or electrolyte restrictions for concomitant conditions - significant cardiovascular event less than or equal to 2 weeks prior to study entry - major surgery less than or equal to 2 weeks prior to study entry - pre-planned surgery during the study period - active malignancy, including melanoma and excluding cutaneous malignancies - severe dementia - known allergies to medical grade adhesives and/or skin disinfectants - taking octreotide - chronic, contagious, infectious disease, such as active tuberculosis, Hepatitis B or C, or HIV - participation in a concomitant trial


NCT ID:

NCT00544206


Primary Contact:

Principal Investigator
Gordon Sacks, PhD
University of Wisconsin, Madison


Backup Contact:

N/A


Location Contact:

Miami, Florida 33161
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 24, 2017

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