Separate and Combined Extrapancreatic Effects of GIP and GLP-1
NCT ID: NCT06895408
Last Updated: 2025-09-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
12 participants
INTERVENTIONAL
2025-02-19
2025-07-14
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
DOUBLE
Study Groups
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GIP
Intravenous infusion of glucose-dependent insulinotropic polypeptide
Intravenous Infusion
Glucose-dependent Insulinotropic Polypeptide
GLP-1
Intravenous infusion of glucagon-like peptide 1
Intravenous Infusion
Glucagon-Like Peptide 1
GIP + GLP-1
Intravenous infusion of glucose-dependent insulinotropic polypeptide and glucagon-like peptide 1
Intravenous Infusion
Glucose-dependent Insulinotropic Polypeptide and Glucagon-Like Peptide 1
Saline
Intravenous infusion of saline
Intravenous Infusion
Saline
Interventions
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Intravenous Infusion
Glucose-dependent Insulinotropic Polypeptide
Intravenous Infusion
Glucagon-Like Peptide 1
Intravenous Infusion
Glucose-dependent Insulinotropic Polypeptide and Glucagon-Like Peptide 1
Intravenous Infusion
Saline
Eligibility Criteria
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Inclusion Criteria
* Caucasians between 30-75 years of age
* Blood haemoglobin \>7.0 mmol/l for males and \>6.5 mmol/l for females
Exclusion Criteria
* Ongoing chemotherapy or chemotherapy within the last 3 months
* Treatment with GLP-1 receptor agonists within the last 3 months
* Renal impairment (estimated by estimated glomerular filtration rate (eGFR) \<60 ml/min/1.73 m2) and/or albuminuria
* Calcium related disease, hypo-/hyperthyroidism
* Known significant liver disease, plasma alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≥3 × normal value or INR (The international normalised ratio based on prothrombin time) outside the normal range
* Severe arteriosclerotic heart disease or heart failure (New York Heart Association (NYHA) group III or IV)
* Pregnancy and/or breastfeeding
* Use of more than 14 units of alcohol per week or abuse of narcotics
* Any condition that the investigator feels would interfere with trial participation
30 Years
75 Years
ALL
No
Sponsors
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University Hospital, Gentofte, Copenhagen
OTHER
Responsible Party
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Asger Lund, MD
Clinical Associate Professor
Locations
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Center for Clinical Metabolic Research, Gentofte Hospital
Hellerup, , Denmark
Countries
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Other Identifiers
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101292 (H-21035117)
Identifier Type: -
Identifier Source: org_study_id
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