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Completed

Liraglutide and Cardio-Metabolic Risk Markers

Effects of Liraglutide on Cardio-Metabolic Risk Markers

Asset

Liraglutide

Subcutaneous · GLP-1 agonist

Listed sites

1

Recruiting sites

Enrollment

300

actual

Study population

Type 2 diabetes

Key I/E criterion

Primary endpoint

Carotid intima-media thickness

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 IDNCT01715428
Org study IDLIRAGLUTIDE UNIPA

Timeline

Milestones

Study first posted2012-10-29estimated
Last update posted2017-11-22actual
Study start2012-06actual (month precision)
Primary completion2015-12actual (month precision)
Study completion2015-12actual (month precision)

Assets

Investigational agents

Study populations

Who this study enrolls

Type 2 diabetes

Eligibility

Who can enroll

Minimum age18 Years
Maximum age80 Years
SexAll
Healthy volunteersNot accepted
Sampling methodProbability sample

Study population text

adult subjects with type-2 diabetes

Inclusion criteria

- patients with a diagnosis of type-2 diabetes

Exclusion criteria

- severe hepatic or renal diseases

Endpoints (4)

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

Cardiometabolic biomarkers
2
Other (unclassified)
2

Cardiometabolic biomarkers

2 endpoints
Primary/protocol endpoint

carotid intima-media thickness

Time frame:every four months for a total period of 2 years

change from baseline, improvement

Secondary/protocol endpoint

changes in atherogenic lipoproteins

Time frame:after 2 and after 4 months of therapy

change from baseline, improvement

Other (unclassified)

2 endpoints
Secondary/protocol endpoint/low confidence

changes in oxidative stress markers

Time frame:after 2 months of therapy

change from baseline, improvement

Secondary/protocol endpoint/low confidence

changes in plasma ghrelin concentrations and heat-shock proteins

Time frame:after 2 months of therapy

change from baseline, descriptive

Publications (6)

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.