Clinical Trials Directory

Trials / Completed

CompletedNCT00660075

Effects of Sitagliptin on Postprandial Lipemia in Men With Type 2 Diabetes

A Randomized, Double-Blind, Placebo-Controlled, Crossover Study To Evaluate The Effects of Sitagliptin on Postprandial Plasma Lipoprotein Concentrations in Men With Type 2 Diabetes

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
36 (actual)
Sponsor
Laval University · Academic / Other
Sex
Male
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Sitagliptin is a potent and selective inhibitor of dipeptidyl peptidase IV (DPP-4), and has been shown to reduce fasting and postprandial glucose levels in patients with type 2 diabetes mainly through incretin hormone-mediated improvements in islet function. Although clinical studies to date indicate that fasting lipid levels are minimally affected by DPP-4 inhibitor treatment, animal studies suggested that DPP-4 inhibition reduce intestinal triglyceride (TG) absorption and apolipoprotein production and increased chylomicron catabolism. Therefore, the present study was designed to examine the effects of sitagliptin on postprandial lipemia in patients with type 2 diabetes. A possible reduction in postprandial atherogenic triglyceride-rich lipoproteins (TRL) levels by sitagliptin would add to therapeutic utility of this DPP-4 inhibitor and suggest the potential to reduce cardiovascular risk in patients with type 2 diabetes.

Conditions

Interventions

TypeNameDescription
DRUGSitagliptinSitagliptin 100 mg/d for 6 weeks
DRUGPlaceboPlacebo for 6 weeks

Timeline

Start date
2008-02-01
Primary completion
2009-01-01
Completion
2009-04-01
First posted
2008-04-17
Last updated
2012-12-11
Results posted
2012-12-11

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00660075. Inclusion in this directory is not an endorsement.

Effects of Sitagliptin on Postprandial Lipemia in Men With Type 2 Diabetes (NCT00660075) · Clinical Trials Directory