LivingGLP1
Study S001719

Acute Effect of a GLP-1-Analogue (Exenatide) and of a DPP-4-Inhibitor (Sitagliptin) in Subjects With Type 2 Diabetes Treated With Insulin Glargine Once Daily

Registration

Registration
NCT00971659
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
48
Start
2008-01
Primary completion
2008-09
Lead sponsor
Profil Institut für Stoffwechselforschung GmbH
Conditions
Type 2 Diabetes
Interventions
DRUG:insulin glargine + exenatide + preexisting metformin; DRUG:insulin glargine + sitagliptin + preexisting metformin; DRUG:insulin glargine + preexisting metformin
Results posted
FALSE

Registered primary outcomes

  • the unadjusted 6-hour postprandial blood glucose excursion (AUCBG0-6h) following ingestion of a standardized breakfast [after 4 weeks of treatment]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0027899Further improvement in postprandial glucose control with addition of exenatide or sitagliptin to combination therapy with insulin glargine and metformin: a proof-of-concept study.
Arnolds S, Diabetes care
2010Randomized trialPMID 20357372DOIcites ClinicalTrials.gov:NCT00971659; registry reference DERIVED:20357372