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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02547337
Other study ID # ISLET-PET
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 10, 2015
Est. completion date June 10, 2021

Study information

Verified date December 2021
Source Turku University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Type 1 diabetes is the major type of diabetes in the young. The pathophysiology still needs clarification in order to reach feasible means of preventing the disease. This study aims in defining the differences in pancreatic and intestinal blood flow between subjects with and without type 1 diabetes and validating the methodology to achieve this. Earlier animal studies have demonstrated changes in pancreatic islet blood flow using microspheres. The aim of this study is to test and validate a method for the assessment of islet perfusion in humans using molecular imaging. The investigators hypothesize that glucose-stimulated pancreatic perfusion is enhanced specifically in islets in healthy subjects and that this increase is mostly suppressed in subjects with type 1 diabetes. Positron emission tomography (PET) is a non-invasive imaging technique, which can be used to study flow and metabolism of different organs. Using radiowater ([15O]H2O) and PET, cellular perfusion can be measured directly and noninvasively. Recently, diffusion weighted magnetic resonance imaging (DWI) has also been applied as a complimentary method for the assessment to quantitate changes in pancreatic blood flow. In the study 10 healthy subjects and 10 subjects with type 1 diabetes will be imaged on two separate days. Pancreatic and intestinal perfusion are first measured with [15O]H2O and combined PET/magnetic resonance imaging before and 5 and 15 minutes after intravenous glucose infusion. On the second day, PET imaging is replaced by dynamic DWI conducted in the same time schedule and with intravenous glucose stimulation.


Recruitment information / eligibility

Status Completed
Enrollment 11
Est. completion date June 10, 2021
Est. primary completion date May 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Criteria for healthy subjects Inclusion criteria - Healthy as judged by history and examination - Age 18-30 years - Body mass index (BMI) 18 - 27 kg/m2 - Normal 2 h oral glucose tolerance test Exclusion criteria - Any chronic disease - Pregnancy - Blood pressure > 140/90 mmHg - Smoking - Presence of any ferromagnetic objects in the body - Any other condition that could possibly create a hazard to the subject safety, endanger the study procedures or interfere with the interpretation of the study results Criteria for subjects with type 1 diabetes (T1D) Inclusion criteria - T1D diagnosed at least 5 years ago - Age 18-30 years - BMI 18 - 30 kg/m2 - Good or moderate glycemic control with long-acting insulin analogue combined with injections of rapid-acting insulin - Uncomplicated T1D or with minor microvascular complications Exclusion criteria - Any other condition or disease possibly affecting circulation, as evaluated by a physician - Pregnancy - Blood pressure > 140/90 mmHg - Smoking - Presence of any ferromagnetic objects in the body - Any other condition that could possibly create a hazard to the subject safety, endanger the study procedures or interfere with the interpretation of the study results

Study Design


Locations

Country Name City State
Finland Turku PET Centre Turku

Sponsors (2)

Lead Sponsor Collaborator
Turku University Hospital Academy of Finland

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pancreatic islet blood flow acquired with PET and DWI (ml ml-1 min-1) healthy subjects and subjects with T1DM are studied once using imaging within one study day
Primary Intestinal blood flow acquired with PET and DWI (ml ml-1 min-1) healthy subjects and subjects with T1DM are studied once using imaging within one study day
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