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Glucagon-like Peptide 2 - a Glucose Dependent Glucagonotropic Hormone? (GLANCE)

U

University Hospital, Gentofte, Copenhagen

Status

Completed

Conditions

Glucose Metabolism Disorders
Endocrine or Metabolic Disease

Treatments

Other: Glucose
Other: Saline
Other: Insulin
Other: Glucagon-like peptide 2

Study type

Interventional

Funder types

Other

Identifiers

NCT03954873
H-18046965

Details and patient eligibility

About

Infusion of glucagon-like peptide 2 (GLP-2) during euglycaemia, hypoglycaemia and hyperglycaemia and evaluation of the effect on glucagon secretion in healthy subjects.

Full description

This is a cross-over, randomized, double-blinded study in which 10 participants will undergo 6 experimental days each. The participants will have their plasma glucose clamped at either euglycaemia (fasting level), hypoglycemia (2,5 mmol/l) or hyperglycemia (10 mmol/l) during infusion of GLP-2 or saline (placebo)

The six days will be as follows:

  • Euglycaemia + Placebo
  • Euglycaemia + GLP-2
  • Hyperglycaemia + Placebo
  • Hyperglycaemia + GLP-2
  • Hypoglycaemia + Placebo
  • Hypoglycaemia + GLP-2

The primary endpoint will be levels of plasma glucagon. Secondary endpoint will be levels of GLP-1, GLP-2, Insulin/C-peptide, OXM, Amino acids, CCK, Gastrin, norepinephrine, bile acids, FGF-19/FGF-21. Secondary endpoints will also include ultrasound scan of the gallbladder.

Enrollment

10 patients

Sex

Male

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Caucasian ethnicity
  • Body mass index (BMI): 18.5-27 kg/m2
  • Glycated haemoglobin (HbA1c) < 42 mmol/mol
  • Normal haemoglobin (8.3-10.5 mmol/l)
  • Informed and oral and written consent

Exclusion criteria

  • Prediabetes, type 1 diabetes or type 2 diabetes or first-degree relatives with type 1 or type 2 diabetes
  • Nephropathy (eGFR < 60 and/or albuminuria)
  • Known liver disease and/or alanine transaminase (ALAT) or aspartate transaminase (ASAT) > 2 × upper normal limit
  • Bilirubin > 25 μmol/l
  • Known intestinal disease or previous surgery of the intestines
  • Active or recent malignant disease
  • Treatment with medicine that cannot be paused for 12 hours
  • Any condition considered incompatible with participation by the investigators

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

10 participants in 6 patient groups

Hyperglycaemia + GLP-2
Experimental group
Description:
Glucose + GLP-2
Treatment:
Other: Glucagon-like peptide 2
Other: Glucose
Hyperglycaemia + Placebo
Active Comparator group
Description:
Glucose + saline
Treatment:
Other: Saline
Other: Glucose
Hypoglycaemia + GLP-2
Experimental group
Description:
Insulin + glucose + GLP-2
Treatment:
Other: Glucagon-like peptide 2
Other: Insulin
Other: Glucose
Hypoglycaemia + Saline
Active Comparator group
Description:
Insulin + glucose
Treatment:
Other: Saline
Other: Insulin
Other: Glucose
Euglycaemia + GLP-2
Experimental group
Description:
GLP-2
Treatment:
Other: Glucagon-like peptide 2
Euglycaemia + Placebo
Active Comparator group
Treatment:
Other: Saline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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