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The aim of this study is to investigate the effects of antagonising GIP after a meal on plasma levels of glucagon. 10 participants are going through four experimental days each, where they ingest a meal and afterwards receive infusions of either GIP receptor antagonist, GLP-1, GIP receptor antagonist + GLP-1 or placebo (saline) in a randomised order. The primary endpoint of the study is plasma levels of glucagon, which we hypothesize will decrease with infusion of GIP receptor antagonist and/or with infusion of GLP-1.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| GIP(3-30)NH2 | Experimental | GIP receptor antagonist |
|
| Placebo | Placebo Comparator | Placebo (saline infusions) |
|
| GLP-1 | Active Comparator |
| |
| GLP-1 + GIP(3-30)NH2 | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| GIP(3-30)NH2 | Other | Peptide derived from the naturally occuring gut hormone GIP |
|
| Measure | Description | Time Frame |
|---|---|---|
| Glucagon | Plasma levels of glucagon after a meal in patients with type 2-diabetes | 8 weeks - 6 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Signe Stensen, MD | Center for Diabetes Research | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Center for Diabetes Research, Gentofte Hospital | Hellerup | 2900 | Denmark |
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| ID | Term |
|---|---|
| C000619446 | gastric inhibitory polypeptide (3-30)-amide |
| D052216 | Glucagon-Like Peptide 1 |
| ID | Term |
|---|---|
| D004763 | Glucagon-Like Peptides |
| D052336 | Proglucagon |
| D005768 | Gastrointestinal Hormones |
| D006728 | Hormones |
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| Peripheral venous cannulation | Other | Intravenous access for infusions |
|
| GLP-1 | Other | Peptide infusion |
|
| D006730 |
| Hormones, Hormone Substitutes, and Hormone Antagonists |