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Effects of Glucagon Like Peptide-1 on Haemodynamic Parameters

Effects of Liraglutide on Hemodynamic Parameters in Patients With Heart Failure

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02490176
Enrollment
50
Registered
2015-07-03
Start date
2015-07-31
Completion date
2016-07-31
Last updated
2016-02-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Brief summary

Glucagon-like peptide-1 (GLP-1) is an incretin hormone that regulates plasma glucose, and GLP-1 analogues were recently introduced for the treatment of acute myocardial infarction. The investigators planned to evaluate the effects of liraglutide on haemodynamic parameters in patients with heart failure.

Detailed description

Heart failure (HF) is a major cause of morbidity and mortality world wide. Glucagon-like peptide-1 (GLP-1) is an incretin hormone that regulates plasma glucose, and has direct effects on the cardiovascular system. In our previous study, the GLP-1 analogue liraglutide could improve left ventricular function in patients with non-ST-segment elevation myocardial infarction. However, the effects of GLP-1 on HF patients remain unclear. Pulse indicator continuous cardiac output (PiCCO) technology is a combination of transpulmonary thermodilution and pulse contour analysis, which measures hemodynamic variables (left ventricular ejection fraction, volumes, and mass) in a fast and feasible way. Therefore, the aim of this study was to evaluate the effects of liraglutide on hemodynamic variables in HF patients using the PiCCO system.

Interventions

DRUGliraglutide

Liraglutide were taken daily for 7 days

DRUGplacebo

Placebo were taken daily for 7 days

Sponsors

Chinese PLA General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

Patients with HF were eligible for the study. Diagnosis of HF was based on an impaired ejection fraction (\<50%).

Exclusion criteria

Patients were also excluded for the following reasons: unconscious at presentation; valvular heart disease, cardiogenic shock, hypoglycaemia, or diabetic ketoacidosis; or renal insufficiency.

Design outcomes

Primary

MeasureTime frameDescription
a change in cardiac output measured by pulse indicator continuous cardiac output (PiCCO) technology7 days after treatmentThe primary efficacy endpoint was the effect of liraglutide on cardiac output (CO) at 7 days compared with placebo.

Secondary

MeasureTime frameDescription
a change in left ventricular contractile index measured by PiCCO technology7 days after treatmentThe change in left ventricular contractile index was measured at 7 days after treatment.

Countries

China

Contacts

Primary ContactWei Ren Chen, M.D.
chen_weiren@sina.com+8610-66939709

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026