NCT01241695

Safety, Acceptability and Efficacy of a Long-term Intervention With a Diabetes-specific Low-carbohydrate, High-mono-unsaturated Fatty Acid Containing Oral Nutritional Supplement on Glycaemic Control in Type 2 Diabetic Patients

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 40 (actual)
• Sponsor: Fresenius Kabi · Industry
• Sex: All
• Age: 40 Years
• Healthy volunteers: Not accepted

Summary

The purpose of the study is to determine the safety, acceptability and the efficacy of a 12-week intervention with a diabetes-specific oral nutritional supplement on glycaemic control in type 2 diabetic patients with or at risk of malnutrition

Conditions

• Diabetes

Interventions

Type	Name	Description
DIETARY_SUPPLEMENT	Oral nutritional supplement, food for special medical purposes	2 servings of 200 ml per day, treatment period: 12 weeks
DIETARY_SUPPLEMENT	Oral nutritional supplement, food for special medical purposes	2 servings of 200 ml per day, treatment period: 12 weeks

Timeline

• Start date: 2010-11-01
• Primary completion: 2011-12-01
• Completion: 2011-12-01
• First posted: 2010-11-16
• Last updated: 2012-07-02

Locations

1 site across 1 country: Germany