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Comparison of A New Technique of Measure of the Insulin Resistance By Scintigraphy With the Reference Technique (GLUCIMAG2)

Primary Purpose

Diabetes Mellitus, Insulin Resistance, Glucose Metabolism Disorders

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
6-DIG
clamp
Sponsored by
Institut National de la Santé Et de la Recherche Médicale, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Diabetes Mellitus focused on measuring insulin resistance, Scintigraphy, Hyperinsulinemic euglycemic clamp

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Insulin sensible patients

    • Body mass index < 25 HOMA <= 2.5
    • Waist measurement < 94 cm for men and < 80 cm for women
    • HDL cholesterol 1,03 mmol/L for men and > 1,29 mmol/L for women
    • Triglyceride level ≤ 1,69 mmol/ L
    • For women not menopausal since at last one year or not surgically sterilised:

On-going contraception, physical or hormonal, excepted local methods (spermicidal, diaphragm, condom, cape)

- Insulin resistant patients

  • For women not menopausal since at last one year or not surgically sterilised:
  • On-going contraception, physical or hormonal, excepted local methods (spermicidal, diaphragm, condom, cape)
  • HOMA > 2.5
  • Body mass index > 25
  • Waist measurement > 94 cm for men and > 80 cm for women
  • HDL cholesterol < 1,03 mmol/L et for men and ≤ 1,29 mmol/L for women
  • Triglyceride level > 1,69 mmol/ L

Exclusion Criteria:

  • • Instable cardiomyopathy

    • Severe hypertension defined by par SAP > 180 mmHg and/or DAP > 110 mmHg
    • Psychiatric illness, needing a chronic treatment
    • Previous history of stroke, epilepsy, cranial trauma, pituitary surgery, disease likely to reduce the ability of absorption, diffusion or excretion of the radiotracer.
    • Allergy to one of the components of the products used during the study
    • Treatment likely to interfere with glucose metabolism
    • Alcohol or drug intoxication
    • Vegetarian or restrictive low-calory diet,
    • Participation in other biomedical research at the same time or exclusion period under another biomedical research
    • Pregnant, parturient or breast-feeding women,
    • Inappropriate way of life

Sites / Locations

  • Hôpital Michallon . CHU Grenoble

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

6-DIG and clamp

Arm Description

injection of 6-DIG and hyperinsulinemic euglycemic clamp

Outcomes

Primary Outcome Measures

Correlation between measure of insulin resistance measurement by scintigraphy and hyperinsulinemic euglycemic clamp
Correlation between measure of insulin resistance measurement by scintigraphy (insulin resistance index: ratio scintigraphy measurement of glucose transport in heart before and after infusion of insulin) and hyperinsulinemic euglycemic clamp (Glucose Infusion Rate and sensibility index Clamp)

Secondary Outcome Measures

SAFETY
A systematic collection of adverse events
Reproducibility
Reproducibility inter and intra operator of Insulin resistance index
Left ventricule ejection fraction
left ventricle volume
cardiac mass
diastolic function
cardiac output
pulmonary pressure and right ventricular function
strain by speckle tracking echocardiography

Full Information

First Posted
March 25, 2014
Last Updated
August 25, 2021
Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
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1. Study Identification

Unique Protocol Identification Number
NCT02102737
Brief Title
Comparison of A New Technique of Measure of the Insulin Resistance By Scintigraphy With the Reference Technique
Acronym
GLUCIMAG2
Official Title
Comparaison d'Une Nouvelle Technique de Mesure de l'insulinorésistance Par Scintigraphie Avec la Technique de référence : Utilisation du 6-DIG Comme Marqueur du Transport du Glucose.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
May 13, 2014 (Actual)
Primary Completion Date
March 2018 (Actual)
Study Completion Date
March 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut National de la Santé Et de la Recherche Médicale, France

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Insulin resistance is closely associated with apparition of type 2 diabetes mellitus; it is an independent risk factor and predicts future cardiovascular events. Hyperinsulinemic euglycemic clamp is a validated method to assessment of insulin resistance and It is also the gold standard technique. However, the complexity and length of this technique render it unsuitable for routine clinical use. In this study, the investigators use a new technique to provide precise, objective, fast and automated quantification of insulin resistance with camera SPECT. They compare the results with those of the measurement of hyperinsulinemic euglycemic clamp in population with or without insulin resistance. The proposed study is to validate this new non-invasive imaging technique for evaluation of insulin resistance in patients with or without insulin resistance with a comparison with hyperinsulinemic euglycemic clamp.
Detailed Description
Currently, type II diabetes mellitus, has reached epidemic levels in the world. Moreover, the prediction for the year 2030 is even more alarming. Insulin resistance, characterized by a depressed cellular sensitivity to insulin in insulin-sensitive organs, is a central feature of the metabolic syndrome and a risk factor for type 2 diabetes. Its appearance may precede the diagnosis of true diabetes several years. Insulin resistance results in decreased membrane translocation of GLUT-4, whole the molecular mechanism remains unclear. Currently, there is no simple tool to measure insulin resistance. The gold standard technique remains the hyperinsulinemic euglycemic clamp. However, the complexity and length of this technique render it unsuitable for routine clinical use. Many methods or index have been proposed to assess insulin resistance in human, but none have shown enough relevance to be used in clinical use. Moreover, all these clinical measurements focus on whole-body glucose uptake, however an accurate and convenient procedure for insulin resistance measurement by organ would be interesting. Indeed there are increasingly evidences to insulin resistance as a primary etiologic factor in the development of nonischemic heart failure (HF), another growing public health problem. Nuclear imaging provides interesting methods to measure insulin resistance using Positron Emission Tomographic (PET) tracer. Two glucose analogs [18F]2-fluoro-2-deoxy-D-glucose (FDG) and [11Cl-30methyl-n-glucose (3-OMG) have been used to evaluate noninvasively the cellular uptake of glucose using PET techniques for several organs like heart, skeletal muscle blood-brain barrier, and liver. [18F] 2-fluoro-2-deoxy-D-glucose (FDG), the most commonly used to study glucose metabolism in humans, allows the estimation of glucose transport and its phosphorylation. A number of kinetic modeling approaches have been used for the quantitation of glucose utilization rates using FDG. FDG is transported and phosphorylated as native glucose, but calculation of glucose uptake and metabolism requires the use of correction factors for each process merged into a lumped constant. The major limitation of these approaches is that quantification of glucose metabolism requires the knowledge of the lumped constant, a factor, which relates the kinetic behavior of FDG to naturally occurring glucose in terms of the relative affinity of each molecule for the trans-sarcolemmal transporter and for hexokinase. Unfortunately, the value of the lumped constant in humans under different physiological and pathophysiological conditions varies, and metabolic imaging with PET need standardization of metabolic conditions by hyperinsulinaemic euglycaemic clamp. 3-OMG appears as an ideal glucose analog to probe transmembrane transport. However, due to the short half-life of the 11C (t1/2 = 20 min), this analog can be used only in clinical institutions in close proximity of a cyclotron and which have access to PET devices. According to these knowledge, the investigators have developed an original compound, [123I] 6-deoxy-6-iodo-D-glucose (6DIG), as a tracer of glucose transport equivalent to 3-OMG, the reference tracer. 6-DIG has previously been exploited to measure IR in vivo and the investigators transfer to human this measurement technique, perfectly validated in animal. Previous, they have reported the first use a potential single-photon emission computed tomography (SPECT) tracer to study basal and insulin-stimulated glucose transport non-invasively. In a phase I of development, they use a new nuclear probe using an iodinated tracer of glucose transport for clinical application and specific imaging processing to assess cardiac insulinoresistance in healthy or diabetic subjects. The results in human subjects show that this technique rapidly provides insulinoresistance index (ratio scintigraphy measurement of glucose transport in heart before and after infusion of insulin) in a simple procedure, opening up new opportunities for screening for pre-diabetic patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Insulin Resistance, Glucose Metabolism Disorders, Metabolic Diseases, Endocrine System Diseases
Keywords
insulin resistance, Scintigraphy, Hyperinsulinemic euglycemic clamp

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
6-DIG and clamp
Arm Type
Experimental
Arm Description
injection of 6-DIG and hyperinsulinemic euglycemic clamp
Intervention Type
Drug
Intervention Name(s)
6-DIG
Intervention Description
injection of 6-DIG
Intervention Type
Procedure
Intervention Name(s)
clamp
Intervention Description
hyperinsulinemic euglycemic clamp
Primary Outcome Measure Information:
Title
Correlation between measure of insulin resistance measurement by scintigraphy and hyperinsulinemic euglycemic clamp
Description
Correlation between measure of insulin resistance measurement by scintigraphy (insulin resistance index: ratio scintigraphy measurement of glucose transport in heart before and after infusion of insulin) and hyperinsulinemic euglycemic clamp (Glucose Infusion Rate and sensibility index Clamp)
Time Frame
DAY 1 AND DAY 2
Secondary Outcome Measure Information:
Title
SAFETY
Description
A systematic collection of adverse events
Time Frame
visit 2, visit 3 and visit 4
Title
Reproducibility
Description
Reproducibility inter and intra operator of Insulin resistance index
Time Frame
day 2 and day 3
Title
Left ventricule ejection fraction
Time Frame
day 2
Title
left ventricle volume
Time Frame
day 2
Title
cardiac mass
Time Frame
day 2
Title
diastolic function
Time Frame
day 2
Title
cardiac output
Time Frame
day 2
Title
pulmonary pressure and right ventricular function
Time Frame
day 2
Title
strain by speckle tracking echocardiography
Time Frame
day 2

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Insulin sensible patients Body mass index < 25 HOMA <= 2.5 Waist measurement < 94 cm for men and < 80 cm for women HDL cholesterol 1,03 mmol/L for men and > 1,29 mmol/L for women Triglyceride level ≤ 1,69 mmol/ L For women not menopausal since at last one year or not surgically sterilised: On-going contraception, physical or hormonal, excepted local methods (spermicidal, diaphragm, condom, cape) - Insulin resistant patients For women not menopausal since at last one year or not surgically sterilised: On-going contraception, physical or hormonal, excepted local methods (spermicidal, diaphragm, condom, cape) HOMA > 2.5 Body mass index > 25 Waist measurement > 94 cm for men and > 80 cm for women HDL cholesterol < 1,03 mmol/L et for men and ≤ 1,29 mmol/L for women Triglyceride level > 1,69 mmol/ L Exclusion Criteria: • Instable cardiomyopathy Severe hypertension defined by par SAP > 180 mmHg and/or DAP > 110 mmHg Psychiatric illness, needing a chronic treatment Previous history of stroke, epilepsy, cranial trauma, pituitary surgery, disease likely to reduce the ability of absorption, diffusion or excretion of the radiotracer. Allergy to one of the components of the products used during the study Treatment likely to interfere with glucose metabolism Alcohol or drug intoxication Vegetarian or restrictive low-calory diet, Participation in other biomedical research at the same time or exclusion period under another biomedical research Pregnant, parturient or breast-feeding women, Inappropriate way of life
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gilles Barone-Rochette, PHU
Organizational Affiliation
Hopital Michalon , CHU de Grenoble
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Michallon . CHU Grenoble
City
Grenoble
ZIP/Postal Code
38043
Country
France

12. IPD Sharing Statement

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Comparison of A New Technique of Measure of the Insulin Resistance By Scintigraphy With the Reference Technique

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