Central Insulin Sensitivity in Individuals With Type 2 Diabetes (T2D) and at Risk for Developing T2D

NCT ID: NCT05856877

Last Updated: 2024-05-14

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 180 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-05-26
• Study Completion Date: 2025-12-31

Brief Summary

Beside well described peripheral effects, insulin can also affect the human central nervous system. Centrally acting insulin seems to have an influence e.g. on whole-body metabolism and food intake. Targeting insulin receptors in the central nervous system can modulate peripheral insulin sensitivity as well as pancreatic insulin secretion. In humans, the effect of insulin can be measured in different brain areas as estimate of central nervous insulin sensitivity. Reduced central nervous insulin sensitivity, called "central insulin resistance," has been associated, for example, with obesity, unfavorable body fat distribution, and impaired cognitive functionality. Recently novel subtypes and risk clusters of diabetes and prediabetes have been identified. In this study the investigators want to investigate and compare central nervous insulin sensitivity as well as cognitive function in the different diabetes and prediabetes risk clusters.

Conditions

Central Insulin Resistance; Diabetes Mellitus, Type 2; PreDiabetes

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: DOUBLE

Study Groups

Nasal insulin spray

Group Type: ACTIVE_COMPARATOR

Human nasal insulin

Intervention Type: OTHER

single dose of 160 U of human insulin as nasal spray

Placebo spray

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Single dose of placebo solution as nasal spray

Interventions

Human nasal insulin

single dose of 160 U of human insulin as nasal spray

Intervention Type: OTHER

Placebo

Single dose of placebo solution as nasal spray

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. manifest diabetes mellitus type 2 with initial diagnosis ≤ 10 years ago, defined as

• a fasting blood glucose greater than 126 mg/dl and/or
• a blood glucose greater than 200 mg/dl at the 120 minute time point in the oral glucose tolerance test with 75 g glucose and/or
• an HbA1c greater than 6.5%

2. or a currently existing increased risk of developing type 2 diabetes, defined as

• prediabetes, defined as

• elevated fasting blood glucose (IFG), fasting blood glucose between 100 and 125 mg/dl) and/or
• impaired glucose tolerance (IGT), 120-minute oral glucose tolerance test blood glucose between 140 and 199 mg/dl) and/or
• HbA1c between 5.7% and 6.4% with
• and/or at least one of the following factors indicating an increased risk for developing type 2 diabetes mellitus:

• previously existing prediabetes and/or
• recent-onset gestational diabetes, and/or
• positive family history (1st degree family members) for type 2 diabetes mellitus and/or
• BMI greater than 27 kg/m2

3. or no manifest diabetes mellitus type 2 and no currently existing increased risk for developing type 2 diabetes (control group: BMI 18.5 to 24.5 kg/m2)

4. female and male (1:1), voluntary adults

5. at least 18 years old and able to give consent

6. understanding of study explanations and instructions

7. consent to information in case of unexpected proven pathological findings.

Exclusion Criteria

• Only in subjects without manifest diabetes mellitus type 2: Taking medications that affect sugar metabolism (e.g., antidiabetic medications or glucocorticoids).
• Diabetes mellitus type 1 or Latent autoimmune diabetes in the adult (GAD and/or IA2 antibodies positive)
• MODY (Maturity onset Diabetes of the Young)
• Decompensated diabetes mellitus type 2 (HbA1c greater than 9.6% and/or fasting blood glucose > 230 mg/dl)
• BMI < 18.5 or > 45 kg/m2
• Individuals wearing non-removable metal devices in or on the body such as:

• pacemakers
• artificial heart valves
• metal prostheses
• implanted magnetic metal parts (screws, plates from surgery)
• coils
• metal splinters/garnet chips
• fixed braces
• retainers going over more than four teeth
• acupuncture needle
• Insulin pump
• intraport
• Tattoos, eye shadow, etc.
• there is a pregnancy or pregnancy cannot be excluded
• breastfeeding women
• Individuals with impaired temperature sensation and/or increased sensitivity to heating of the body.
• symptomatic coronary heart disease, heart failure greater than NYHA 3, previous heart attack
• Condition following stroke
• Individuals with hearing disease or increased sensitivity to loud sounds
• Persons with claustrophobia (fear of place)
• Minors or subjects incapable of giving consent
• Subjects who have had an operation less than 3 months ago
• Acute illness or infection within the last 4 weeks
• Severe neurological or psychiatric diseases, e.g. severe depression (at least 29 points according to BDI II), schizophrenia or bipolar disorder.
• Use of centrally acting drugs
• Known presence of malignant disease within the last 5 years
• Diseases of the pancreas
• Systemic infection (CRP > 1 mg/dl)
• Following bariatric surgery
• Antibiotic therapy within the last 4 weeks prior to study inclusion
• No consent to be informed about incidentally discovered pathological findings
• Participation in interventional trials and receipt of investigational medication in the last 30 days
• Severe diabetic complications such as chronic kidney disease (KDIGO CKD greater than G4) or severe proliferative retinopathy
• Subjects with hemoglobin levels Hb<10.5g/dl (for women), Hb<11.5g/dl (for men)
• Other medical conditions that, in the opinion of an investigator, may jeopardize the success of the study or indicate that the subject may be at risk of harm
• Allergic diseases to any of the substances used

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University Hospital Tuebingen

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

University Hospital Tübingen

Tübingen, , Germany

Site Status: RECRUITING

Countries

Germany

Central Contacts

Stephanie Kullmann, Prof.

Role: CONTACT

stephanie.kullmann@med.uni-tuebingen.de

070712987702

Christian Kübler, Dr.

Role: CONTACT

christian.kuebler@med.uni-tuebingen.de

070712968784

Other Identifiers

INCLU

Identifier Type: -

Identifier Source: org_study_id