Recruitment

Recruitment Status
Completed
Estimated Enrollment
35

Summary

Conditions
Type 2 Diabetes
Type
Interventional
Phase
Phase 4
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Hypotheses Primary hypothesis • Liraglutide treatment causes a reduction in 24h BP Secondary hypothesis: The effect on BP may be mediated by an increase in natriuresis, thereby affecting ECV The effect on BP may be mediated by a decrease in arterial stiffness and central aortic pressure Purpose Prim...

Hypotheses Primary hypothesis • Liraglutide treatment causes a reduction in 24h BP Secondary hypothesis: The effect on BP may be mediated by an increase in natriuresis, thereby affecting ECV The effect on BP may be mediated by a decrease in arterial stiffness and central aortic pressure Purpose Primary purpose • To assess how quickly the antihypertensive effect of liraglutide treatment set in after initiation in patients with type 2 diabetes Secondary objectives To measure the effect of liraglutide treatment on natriuresis. To measure the effect of liraglutide treatment on ECV To measure the effect of liraglutide treatment on arterial stiffness To measure weight change after initiation of liraglutide treatment

Tracking Information

NCT #
NCT01499108
Collaborators
Novo Nordisk A/S
Investigators
Principal Investigator: Peter Rossing, MD Steno Diabetes Centes