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LIRABONE

CompletedPhase 4

The Effect of Liraglutide on Bone Turnover, Bone Mass and Bone Cell Function

Asset

Liraglutide

Subcutaneous · GLP-1 agonist

Listed sites

1

Recruiting sites

Enrollment

60

actual

Study population

Type 2 diabetes

Key I/E criterion

Primary endpoint

Collagen I cross-linked C-terminal telopeptide measured in serum

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 IDNCT02473809
Org study ID07052015

Timeline

Milestones

Study first posted2015-06-17estimated
Last update posted2018-09-26actual
Study start2015-08 (month precision)
Primary completion2017-10actual (month precision)
Study completion2017-10actual (month precision)

Assets

Investigational agents

Study populations

Who this study enrolls

Type 2 diabetes

Eligibility

Who can enroll

Minimum age30 Years
Maximum age90 Years
SexAll
Healthy volunteersNot accepted

Inclusion criteria

Informed consent
Diagnosis of type 2 diabetes (HbA1c > 48 mmol/mol)
Age older than 30 years

Exclusion criteria

Type 1 diabetes
Treatment with insulin
Body weight > 140 kg
HbA1c > 75 mmol/mol
Treatment with GLP-1 analogues, Dipeptidyl peptidase-4 inhibitors, or glitazones
Chronic kidney disease
Hepatic disease
Pancreatitis
Inflammatory bowel disease
Osteoporosis
Family or personal history of medullary thyroid carcinoma
Treatment with glucocorticoids
Hormone replacement therapy
Diabetic gastroparesis
Pregnancy or lactation

Endpoints (7)

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

Other (unclassified)
3
Other clinical outcomes
2
Weight & body composition
1
Glycemic / diabetes
1

Weight & body composition

1 endpoint
Secondary/protocol endpoint

Change in BMD evaluated by DXA

Time frame:Days 0, 90, 180

change from baseline, improvement

Glycemic / diabetes

1 endpoint
Secondary/protocol endpoint

Change in HbA1c

Time frame:Days 0, 180

HbA1c, change

change from baseline, improvement

LOINC 4548-4

Other clinical outcomes

2 endpoints
Primary/protocol endpoint

Change in collagen I cross-linked C-terminal telopeptide measured in serum

Time frame:Days 0, 7, 28, 90, 180

change from baseline, improvement

Secondary/protocol endpoint/low confidence

Change in bone structure evaluated by QCT and HRpQCT

Time frame:Days 0, 90, 180

change from baseline, improvement

Other (unclassified)

3 endpoints
Secondary/protocol endpoint/low confidence

Change in bone alkaline phosphatase measured in serum

Time frame:Days 0, 7, 28, 90, 180

change from baseline, descriptive

Secondary/protocol endpoint/low confidence

Change in osteocalcin measured in serum

Time frame:Days 0, 7, 28, 90, 180

change from baseline, improvement

Secondary/protocol endpoint/low confidence

Change in procollagen type I N-terminal propeptide measured in serum

Time frame:Days 0, 7, 28, 90, 180

change from baseline, improvement

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.