Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Buffalo, New York 14221


Purpose:

Sitagliptin is a new oral hypoglycemic anti-diabetic drug used either alone or in combination with metformin or a thiazolidinedione for control of type 2 diabetes mellitus. Sitagliptin has been shown to have fewer side effects in the control of blood glucose values. Obesity and diabetes are states of increased inflammation and can influence the free radicals and inflammatory markers (chemicals in the blood which increase due to inflammation in the body) and are also major risk factors for atherosclerotic disease. In this study we want to see the effect of sitagliptin on these markers. We believe that Sitagliptin may exert an anti-inflammatory effect in the human. The purpose of this study is to determine if the addition of sitagliptin to diabetic patients will provide added benefit. We believe that sitagliptin provides these added benefits by suppressing free radicals (charged substances that cause damage to the body) and inflammation.


Criteria:

Inclusion Criteria: - Males or females with age 20-75 years inclusive. - Type 2 diabetes - Males and Females BMI > 30 - Subjects on statins, ACE inhibitors, thiazolidenediones and antioxidants will be allowed as long as they are on stable doses of these compounds and the dosage in not changed during the course of study. - BP under control -No change required to BP medications - HbA1c > 7% Exclusion Criteria: - Coronary event or procedure (myocardial infarction, unstable angina, coronary artery bypass, surgery or coronary angioplasty) in the previous four weeks - Pregnancy - Hepatic disease (abnormal LFT's),Renal impairment (serum creatinine > 1.5), - Participation in any other concurrent clinical trial - Any other life-threatening, non-cardiac disease, - Uncontrolled hypertension (BP > 160/100 mm of Hg) - Congestive Heart Failure - Use of an investigational agent or therapeutic regimen within 30 days of study - Subjects on Exenatide, incretin or insulin therapy


NCT ID:

NCT00659711


Primary Contact:

Principal Investigator
Paresh Dandona, MD
Kaleida Health


Backup Contact:

N/A


Location Contact:

Buffalo, New York 14221
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: February 04, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.