Overview
Delineation of the Role of Glucagon-like Peptide-1 Signalling in Relation to Increased Carbohydrate Content in the Distal Small Intestines
Status:
Completed
Completed
Trial end date:
2018-01-01
2018-01-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
Investigation of GLP-1 signalling in the glucose-lowering effect of increased carbohydrate content in the distal small intestines induced by alpha-glucosidase inhibition during meal ingestion in patients with type 2 diabetesPhase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
University Hospital, Gentofte, CopenhagenCollaborator:
University of CopenhagenTreatments:
Acarbose
Glucagon
Glucagon-Like Peptide 1
Criteria
Inclusion Criteria:- Type 2 diabetes for at least three months (diagnosed according to the criteria of the
World Health Organization (WHO)) treated with metformin monotherapy
- Caucasian ethnicity
- Normal haemoglobin
- Age >18 years
- BMI >23 kg/m2 and <35 kg/m2
- Informed and written consent
Exclusion Criteria:
- Liver disease (alanine aminotransferase (ALAT) and/or serum aspartate aminotransferase
(ASAT) >2 times normal values) or history of hepatobiliary disorder
- Gastrointestinal disease, previous intestinal resection, cholecystectomy or any major
intra-abdominal surgery
- Reduced kidney function or nephropathy (estimated glomerular filtration rate (eGFR)
<60 ml/min/1.73 m2 (based on serum creatinine) and/or albuminuria
- Treatment with medicine that cannot be paused for 12 hours
- Intake of antibiotics two months prior to study
- Treatment with glucose-lowering drugs other than metformin
- Hypo- and hyperthyroidism
- Treatment with oral anticoagulants
- Active or recent malignant disease
- Any treatment or condition requiring acute or sub-acute medical or surgical
intervention
- Lack of effective birth control in premenopausal women
- Positive pregnancy test on study days in premenopausal women
- Pregnancy
- Women who are breastfeeding
- Any condition considered incompatible with participation by the investigators
- If the subjects receive any antibiotic treatment while included in the study they will
be excluded