Effect of Nutritional Products in Subjects With Type 2 Diabetes

Completed · Not applicable

Conditions studied: Diabetes

In brief

This is a randomized, double blinded, multi treatment, crossover study intended to compare the glycemic and insulinemic response after consuming liquid nutritional products in people with type 2 diabetes.

Key facts

Study ID: NCT02923960
Run by: Abbott Nutrition
People needed: 43
Starts: 2016-10-01
Expected to finish: 2017-01-01
Last updated by the study team: 2017-04-17

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: accepted.

You may qualify if…

Subject has type 2 diabetes
Subject is a male or a nonpregnant, nonlactating female, at least 6 weeks postpartum prior to screening visit
Subject's BMI is > 18.5 kg/m2 and < 35 kg/m2
If on a chronic medication such as antihypertensive, lipid lowering, thyroid medication or hormone therapy, subject has been on constant dosage for at least two months prior to screening visit
Subject states willingness to follow protocol as described, including consumption of study product per protocol and completing any required study forms
Participant must refrain from taking medications/dietary supplements/herbals or substances that could modulate glucose metabolism (other than oral hypoglycemic medications), or considered anabolic, or reduce weight (fat mass)

You may not qualify if…

Subject is currently diagnosed with, or has a history of severe dementia or delirium, eating disorder, history of significant neurological or psychiatric disorder, alcoholism, substance abuse or other conditions that may interfere with study product consumption or compliance with study protocol procedures
Subject is known to be allergic or intolerant to any ingredient found in the study products
Subject is participating in another study that has not been approved as a concomitant study
Subject uses exogenous insulin for glucose control, or subject states that they have been diagnosed as having Type 1 diabetes
Subject states they have a history of diabetic ketoacidosis
Subject is currently on a low carbohydrate or very low carbohydrate diet
Subject states that he/she has a current infection; has had inpatient surgery, or corticosteroid treatment in the last 3 months or antibiotics in the last 3 weeks prior to screening visit
Subject states that he/she has an active malignancy
Subject states that he/she has had a significant cardiovascular event ≤ six months prior to screening visit; or stated history of congestive heart failure
Subject states that he/she has end stage organ failure or is status post organ transplant
Subject is diagnosed with chronic kidney disease, or a history of kidney issues
Subject states they have impaired liver function, or have a history of liver disease
Subject has an obstruction of the gastrointestinal tract precluding ingestion of the study product, inflammatory bowel disease, short bowel syndrome or other severe forms of gastrointestinal disease such as gastroesophageal reflux disease, gastroparesis, peptic ulcer disease, celiac disease, intestinal dysmotility, diverticulitis, or ischemic colitis, or any other related condition that may cause unnecessary subject discomfort
Subject states they have a chronic, contagious, infectious disease
Subject has taken/is currently taking any herbals, dietary supplements, or medications during the past four weeks prior to screening visit that are designed to affect blood glucose.
Subject states that he/she has clotting or bleeding disorders
If selected for continuous blood glucose monitoring, subject has skin lesions, hyperhidrosis, eczema, psoriasis, scarring, redness, infection or edema at the flash constant glucose monitoring application site(s) that could interfere with device placement or the accuracy of interstitial glucose measurements.
If selected for continuous blood glucose monitoring, subject has an X-ray, MRI or CT appointment scheduled during the period of study participation, or another procedure that would require removal of the flash constant glucose monitoring sensor.
Subjects on sulfonylureas, meglitinides, and α-glucosidase inhibitors, insulin, or subject on more than two oral hypoglycemic medications excluding aforementioned.
Subjects on oral hypoglycemic medications that has changed in last 2 months.
Subject's HbA1c, per point of care device is > 8%

Where it is running

Great Lakes Clinical Trials — Chicago, Illinois, United States
Radiant Research, Inc. — Cincinnati, Ohio, United States

Full record on ClinicalTrials.gov

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