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The Role of GIP in Postprandial Splanchnic Blood Flow Distribution and Metabolism in Patients With Type 2 Diabetes

The Role of GIP in Postprandial Splanchnic Blood Flow Distribution and Metabolism in Patients With Type 2 Diabetes

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06426823
Acronym
GA-17b
Enrollment
10
Registered
2024-05-23
Start date
2023-11-01
Completion date
2026-03-16
Last updated
2026-03-18

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

Conditions

Blood Flow

Keywords

Gut hormones, GIP, Physiology, Type 2 diabetes

Brief summary

This project will describe the mechanisms of action and the relative contributions of GIP to changes in gastrointestinal blood flow induced by oral glucose and endogenous GIP with the use of a receptor antagonists GIP(3-30)NH2 in patients with type 2 diabetes.

Detailed description

Each participant will attend four independent randomised experimental days in the MRI-scanner with intravenous infusion (hormone/placebo) and oral ingestion (glucose/water): An intravenous infusion of saline or GIP(3-30)NH2 starts at time point -20 minutes.The infusions are combined with an oral glucose tolerance test (75 gram of glucose dissolved in 250 ml water ingested orally) at time point 0 minutes on two of the experimental days (with and without GIP(3-30)NH2). MRI measurements are repeatedly performed and blood samples are drawn to be analysed for endocrine responses from the intestines, pancreas, and bones.

Interventions

OTHERSaline / placebo

NaCl (9 mg/ml)

Sponsors

University of Copenhagen
Lead SponsorOTHER
Rigshospitalet, Denmark
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Intervention model description

Single blind, placebo controlled, randomized, crossover study

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Type 2 diabetes * BMI 20-35 kg/m\^2 * Age 20-80

Exclusion criteria

* Not MRI-compatible implants * Claustrophobia * Abnormal kidney or liver function * Anemia * Planned weight loss or change in diet * Hypertension * Other conditions that could be expected to affect the primary or secondary outcomes

Design outcomes

Primary

MeasureTime frameDescription
Redistribution of splanchnic blood flow in the vessel mesenteric superior artery (functional MRI)80 minutesMeasued with phase-contrast MRI in ml/min

Secondary

MeasureTime frameDescription
GIP levels80 minutesRadioimmuno assay on plasma blood sample (pmol/L)
GIP(3-30)NH2 levels80 minutesRadioimmuno assay on plasma blood sample (nmol/L)
C-peptide80 minutesElectrochemiluminescence immunoassay of plasma blood sample (pmol/L)
Insulin80 minutesElectrochemiluminescence immunoassay of plasma blood sample (pmol/L)
Glucagon80 minutesRadioimmuno assay on plasma blood samples (pmol/L)
Blood flow in portal vein80 minutesMeasued with phase-contrast MRI in ml/min
Blood flow in coeliac trunc80 minutesMeasued with phase-contrast MRI in ml/min
Glucose80 minutesBedside measurement of whole blood sample (mmol/L)
Blood flow in hepatic artery80 minutesMeasued with phase-contrast MRI in ml/min

Countries

Denmark

Outcome results

None listed

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