LivingGLP1
Study S002027

Safety Evaluation of Adverse Reactions in Diabetes

Registration

Registration
NCT02092597
Acronym
SAFEGUARD
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE4
Masking
NONE
Status
COMPLETED
Enrollment
42
Start
2013-10
Primary completion
2015-10
Lead sponsor
Charles University, Czech Republic
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:Exenatide; DRUG:Linagliptin; DRUG:Gliclazide
Results posted
FALSE

Registered primary outcomes

  • Heart rate [90 days after treatment initiation]
  • Gastric evacuation velocity [90 days after treatment initiation]
  • Blood pressure [90 days after treatment initiation]
  • Left ventricular ejection fraction [90 days after treatment initiation]
  • Intimomedial thickness [90 days after treatment initiation]
  • Pulse wave velocity [90 days after treatment initiation]
  • Glomerular filtration rate [90 days after treatment initiation]
  • Tubular function [90 days after treatment initiation]
  • KIM-1 [90 days after treatment initiation]
  • Exocrine pancreas function [90 days after treatment initiation]

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