Study of a Carbohydrate Drink in Adults
Completed · Not applicable
Conditions studied: Glycemic Response
In brief
The objective of this study is to determine the postprandial glycemic response and rates of gastric emptying in healthy subjects and those with pre-diabetes and type 2 diabetes following oral ingestion of carbohydrate.
Key facts
- Study ID
- NCT04313920
- Run by
- Abbott Nutrition
- People needed
- 97
- Starts
- 2020-04-07
- Expected to finish
- 2020-08-26
- Last updated by the study team
- 2020-10-06
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Subject has voluntarily signed and dated an informed consent form and provided Health Insurance Portability and Accountability Act (HIPAA) authorization
- Subject is healthy or has pre-diabetes or type 2 diabetes
- Subject is a male or a non-pregnant, non-lactating female, at least 6 weeks postpartum
- Subject's BMI is > 18.5 kg/m2 and ≤ 40.0 kg/m2
- If subject is on a chronic medication, the dosage has been constant
- Subject states willingness to follow protocol
You may not qualify if…
- Subject uses exogenous insulin or Glucagon-like peptide-1 (GLP-1) receptor agonists for glucose control
- Subject has type 1 diabetes
- Subject has a history of diabetic ketoacidosis
- Subject has current infection; has had in-patient surgery, or corticosteroid treatment or antibiotics
- Subject has an active malignancy
- Subject has had a significant cardiovascular event ≤ six months or history of congestive heart failure
- Subject has end-stage organ failure or is status post organ transplant.
- Subject has a history of renal disease
- Subject has current hepatic disease
- Subject has a history of severe gastroparesis
- Subject has a chronic, contagious, infectious disease
- Subject has taken/is currently taking any herbals, dietary supplements, or medications that could profoundly affect blood glucose
- Subject has clotting or bleeding disorders
- Subject is known to be allergic or intolerant to any ingredient found in the study products
- Subject is a participant in another study that has not been approved as a concomitant study
Where it is running
- Health Awareness, Inc. — Jupiter, Florida, United States
- Biofortis — Addison, Illinois, United States
- Great Lakes Clinical Trials — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.