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The Effect of Liraglutide on Pancreatic Hormones and Its Size

The Effect of Liraglutide on Pancreatic Hormones and Its Size

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03520062
Acronym
LIRAP
Enrollment
14
Registered
2018-05-09
Start date
2017-08-15
Completion date
2020-01-01
Last updated
2020-03-24

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

Conditions

Obesity

Keywords

Amylase, Lipase, GLP-1

Brief summary

Glucagon-like peptide-1 (GLP-1) is a gastrointestinal hormone used to treat type 2 diabetes and severe overweight (Liraglutide).The two pancreas enzymes: amylase and lipase are slightly elevated in GLP-1 treated compared with placebo-treated individuals. Increased levels of these two enzymes (amylase and lipase) are associated with acute inflammation of the pancreas (acute pancreatitis). In humans treated with GLP-1 (receptor agonist) there have not been found an increased risk of acute pancreatitis. Animal and cell studies have shown that the increased levels of amylase and lipase in the blood are not due to an inflammatory state but adaptive changes (volume increase) of the pancreas. The investigators (professor Jens Juul Holst, professor Sten Madsbad) want to investigate whether the increased levels of amylase and lipase in the blood of individuals treated with the GLP-1 analogue Saxenda are due adaptive changes of the pancreas. This will be achieved by measuring amylase and lipase before, during and after treatment with a GLP-1 receptor agonist, and at the same time use advanced scanning equipment (PET-MR) from the Clinical Physiological and Nuclear Medical Department at Rigshospitalet, which can determine any volumetric changes in the pancreas with high reproducibility. The scan will be centered on the pancreas, other organs are not evaluated why the study is not designed to detect any malignant findings in the pancreas or other organs.

Interventions

Treatment with Liraglutide (3.0mg per day) for \ 6 weeks

Sponsors

Hvidovre University Hospital
CollaboratorOTHER
Rigshospitalet, Denmark
CollaboratorOTHER
Nicolai Jacob Wewer Albrechtsen
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* BMI ≥ 26 og \< 50 kg/m2

Exclusion criteria

* Abdominal Diameter \>60cm type 1 or type 2 diabetes Heart Failure or Disease Statins Kidney or Liver disease Thyroid Disease Inflammatory Bowel Disease Gastroparesis Cancer Lung disease Psychiatric disease Gastric Bypass operation Previous pancreatitis Increased alcoholic consumption Familiar incidence of multiple endocrine neoplasia Previous treatment with GLP-1 (incretin) based medicine Pacemaker or other non-MR-compatible devices

Design outcomes

Primary

MeasureTime frameDescription
Volumetric Changes of the Pancreas6 weeksMeasurements of the pancreas volumen using magnetic resonance imaging-positron emission tomography based technology

Secondary

MeasureTime frame
Changes in body weight6 weeks
Changes in glycemic index6 weeks
Plasma concentrations of glucagon, insulin and citrullin6 weeks
Changes in Plasma Concentrations of Pancreatic Amylase and Lipase6 weeks
Other MR based changes in the pancreas (edema, cellularity and structural changes)6 weeks
Uptake of fluorothymidine tracer in the pancreas measured by PET4 weeks
Plasma concentrations of the drug6 weeks

Countries

Denmark

Outcome results

None listed

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