Vildagliptin
Drug50mg vildagliptin bid
NCT Number: NCT01398592
This study is designed to assess the potential difference in Fasting Plasma Glucose (FPG) lowering efficacy between the two DPP-4 inhibitors vildagliptin and sitagliptin, both after a two weeks treatment on top of metformin.
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Notify Me18 year–85 year
All sexes
Interventional
Phase 4
Novartis Investigative Site, Bad Oeynhausen, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patients with type 2 diabetes 18 to 85 years Metformin monotherapy > 4 weeks HbA1c 6.5 - 9.5%
Exclusion criteria
FPG > 270 mg/dl Use of other antidiabetic drugs than metformin major cardiovascular event in the last 6 months (MI, stroke…)
50mg vildagliptin bid
100mg sitagliptin po qd
Time frame: 14 days
Fasting Plasma Glucose measured on day 14.
Time frame: 14 days
Fasting Plasma Glucose on day 14 analyzed descriptively.
Novartis Pharmaceuticals
Industry
Cross-over Study to Assess the Difference in Fasting Plasma Glucose (FPG) Between Vildagliptin (Galvus®/Eucreas®) and Sitagliptin (Januvia®/Janumet®) After Two Weeks
Acronym: FPG-VISIT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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