← Trials/Trial dossier/NCT02490176

UnknownPhase NA

Effects of Glucagon Like Peptide-1 on Haemodynamic Parameters

Effects of Liraglutide on Hemodynamic Parameters in Patients With Heart Failure

Asset

Liraglutide

Subcutaneous · GLP-1 agonist

Listed sites

1

Recruiting sites

1

Enrollment

50

estimated

Study population

Heart failure

Key I/E criterion

EF ≤50%

Primary endpoint

A change in cardiac output

Footprint

Where this trial recruits

Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT02490176
Org study IDS2015-095-01

Timeline

Milestones

Study first posted2015-07-03estimated
Last update posted2016-02-29estimated
Study start2015-07 (month precision)
Primary completion2016-07estimated (month precision)
Study completion2016-07estimated (month precision)

Assets

Investigational agents

Study populations

Who this study enrolls

Heart failure

Eligibility

Who can enroll

Minimum age18 Years
Maximum age80 Years
SexAll
Healthy volunteersNot accepted

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.

Endpoints (2)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

Coverage by outcome category

Heart failure
1
Other (unclassified)
1

Heart failure

1 endpoint
Primary/protocol endpoint

a change in cardiac output measured by pulse indicator continuous cardiac output (PiCCO) technology

Time frame:7 days after treatment

change from baseline, improvement

Other (unclassified)

1 endpoint
Secondary/protocol endpoint/low confidence

a change in left ventricular contractile index measured by PiCCO technology

Time frame:7 days after treatment

change from baseline, descriptive

Publications (7)

Bibliography

Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.

Registry references + supporting bibliography

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.