CClinicalTrials.gg
CompletedNCT04178603COBOSUpdated Jan 6, 2022

Copenhagen, Boston, Sydney

An interventional study of Exercise, insulin infusion in Insulin Resistance, Insulin Sensitivity and Type 2 Diabetes, sponsored by University of Copenhagen. Completed at 1 site in Denmark. Open to male participants aged 25 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-01-06.

Sponsored by University of Copenhagen · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 1 year 4 months after the study started (first participant enrolled Jul 2018, registered Nov 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
21
Allocation
Non-randomized
Ages
25 Years to 40 Years
Sex
Male
01

Study summary

The study investigates the regulation of muscle glucose utilization during exercise and enhanced insulin sensitivity in recovery from exercise.

This will be investigated in lean control subjects and obese insulin resistant subjects.

Read the detailed description

The subjects will perform two trials (trial A and B).

Trial A: During trial A the study subject will eat a morning meal at 6:00 a.m. corresponding to 5% of the daily energy requirements and will arrive at the research laboratory at 8:00 a.m. It is requested that the study subject will arrive in a car or with public transportation. After arrival the study subject will rest for 1 hour and at that time catheters are inserted in both femoral veins and the femoral artery in one of the legs. At 9:00 a.m. the study subjects will perform one-leg knee extension exercise for 1 hour at an intensity of 80% of maximal work capacity. In this work protocol there are inserted 3 intervals of 5 minutes duration where the study subject works at 100% of maximal intensity with the purpose of securing a full activation/recruiting of all muscle fibers. Muscle biopsies from the m. vastus lateralis muscle in both legs will be taken before (at 8.45 a.m.), immediately after (at 10:00 a.m.) and 2 hours after conclusion of exercise (at 12:00 p.m.) (in total of 6 biopsies). Pulmonary oxygen uptake is measured with the use of an online system before, during and after exercise and is used for determination of substrate metabolism. Blood samples from the femoral veins in both legs and the femoral artery in one of the legs are drawn before (at 8:20 a.m., 8:40 a.m. and 9:00 a.m.), during exercise (at 9:20 a.m., 9:40 a.m. and 10:00 a.m.) and during the recovery period after exercise (at 10:10 a.m., 10:30 a.m., 11:00 a.m., 11:30 a.m. and 12:00 p.m.). At the same time blood flow is measured in the femoral arteries in both legs with the use of Doppler technique. Determination of arteriovenous difference (AV difference) by simultaneous measurement of blood flow enables us to calculate skeletal muscle glucose uptake and uptake/release of relevant substances (proteins, peptides and metabolites etc.). The experimental part of trial A is completed at 12:00 p.m. The study subject will be given food and drink and will be observed for one hour before they may leave the research laboratory.

Trial B: During test trial B the study subjects will eat a morning meal at 6:00 a.m. corresponding to 5% of the daily energy requirements and will arrive at the research laboratory at 8:00 a.m. It is requested that the study subject will arrive in a car or with public transportation.

During trial B the study subjects will perform the same one-leg knee extension exercise protocol as in trial A. At 9:00 a.m. the study subject starts performing one-leg knee extension exercise for 1 hour at 80% of maximal work capacity with 3 intervals of 5 minutes duration where the load is at 100% of maximal work capacity. This work protocol ensures full activation/recruiting of all muscle fibers. After the kicking exercise is completed the study subject will rest in supine position for 6 hours. At the beginning of this resting period catheters are inserted in the femoral veins in both legs and in the femoral artery in one leg. Also catheters are inserted in each forearm vein (antecubital veins) for intravenous infusion of insulin, glucose and stable 13C(u)-glucose. Intravenous infusion of 13C(u)-glucose is started 2 hours after conclusion of exercise in order to achieve a 10% enrichment of blood glucose. 4 hours after cessation of exercise a hyperinsulinemic euglycemic clamp of 120 minutes duration is started. This implies intravenous infusion of insulin and glucose for 120 minutes in order to determine insulin sensitivity for glucose uptake and metabolism of glucose. The clamp is started with a bolus injection of insulin (9.0 mU/kg) followed by a constant infusion (1.42 mU/kg/min). Simultaneously glucose infusion rate will be adjusted so that euglycemia is maintained. Immediately before, after 30 minutes and after 120 minutes of insulin infusion a muscle biopsy is taken from the vastus lateralis muscle in both legs (a total of 6 biopsies). Blood samples from both femoral veins and one femoral artery are taken before (at 12:00 p.m., 12:30 p.m., 1:00 p.m., 1:30 p.m. and 2:00 p.m.) and during (at 2:15 p.m., 2:30 p.m., 2:45 p.m., 3:00 p.m., 3:15 p.m., 3:30 p.m., 3:45 p.m. and 4:00 p.m.) the hyperinsulinemic euglycemic clamp. Simultaneously blood flow is measured in both femoral arteries with use of Doppler technique. Determination of arteriovenous difference (AV difference) by simultaneous measurement of blood flow enables us to calculate glucose uptake and uptake/release of relevant substances (proteins, peptides and metabolites etc.). Indirect calorimetry for determination of whole body metabolism is measured concomitantly, starting 2 hours after conclusion of exercise. The experimental part of trial B is concluded at 4:00 p.m. The study subjects receive food and drink and are observed for one hour before they may leave the research laboratory.

Muscle biopsies and blood samples from trial A and B are stored in a locked -80ºC freezer. Muscle samples and blood samples will subsequently be used for miscellaneous analyses described under background.

The trials (A and B) will be carried out in a randomized order and will be separated by a minimum of 14 days.

02

Conditions studied

  • Insulin Resistance
  • Insulin Sensitivity
  • Type 2 Diabetes

Keywords

  • Exercise
  • Insulin Resistance
  • Type 2 Diabetes
  • Glucose Uptake
  • Insulin Sensitivity
03

In context

Diabetes Mellitus, Type 2

9,359 studies on the registry are indexed under Diabetes Mellitus, Type 2; 1,318 are open to participants now.

This study's enrollment of 21 is below the median of 80 across 7,525 interventional studies indexed under Diabetes Mellitus, Type 2.

Browse Diabetes Mellitus, Type 2 studies →

Lead sponsor

University of Copenhagen is the lead sponsor of 450 studies on the registry; 61 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 40 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria for Study Subjects

  • Healthy persons (no known disease) without diabetes in the family
  • No use of medications
  • Non-smokers
  • Men
  • Age 25-40 years
  • Physical activity level (VO2peak) between 30-50 mL O2/min/kg

Specific for the persons of normal weight:

  • BMI between 18.0 and 25.0
  • HOMA-IR ≤ 1.5
  • Glucose tolerant (intact response in relation to oral glucose tolerance test, OGTT)
  • Without metabolic syndrome (defined by the International Diabetes Federation in 2006)

Specific for the persons with overweight and insulin resistance:

  • BMI between 28.0 and 35.0
  • HOMA-IR ≥ 2.2
  • Glucose tolerant (intact response in relation to OGTT)

Exclusion criteria

  • Women
  • Elevated blood pressure (systolic above 140 mmHg, diastolic above 90 mmHg).
  • Persons who show signs of metabolic diseases, hematologic diseases, reduced liver function or other signs of disease that may affect the outcome of the study or the study subject's wellbeing will be excluded.

Exclusion after Inclusion

  • If disease appears or is identified and/or a need for medication arises after inclusion but before initiation of the study.
  • Disease during conclusion of the study
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
21 participants (actual)

Study arms

  • Experimental
    Acute Exercise Trial

    Lean control subjects and insulin resistant subjects perform an acute bout of one-legged knee-extensor exercise. Glucose metabolism is investigated before exercise (basal), during exercise and for 120 min of recovery.

    Other: Exercise, insulin infusion

  • Experimental
    Insulin Sensitivity post Exercise

    Lean control subjects and insulin resistant subjects perform an acute bout of one-legged knee-extensor exercise and insulin action is investigated 4 hours after cessation of exercise. Insulin action is investigated by a 120 min euglycemic-hyperinsulinemic euglycemic clamp.

    Other: Exercise, insulin infusion

Interventions

  • OtherExercise, insulin infusion

    Trial A: Acute one-legged exercise Trial B: Insulin infusion 4 hours after one-legged exercise

06

What researchers measure

Primary outcomes

  1. Muscle glucose uptake during exercise and enhanced insulin sensitivity in recovery from exercise.

    Muscle glucose uptake during exercise and during insulin stimulation in recovery from exercise (insulin sensitivity) will be determined based on the the Fick principle. Thus, arterio-venous difference (av difference) in blood glucose will be multiplied by arterial leg blood flow.

    Time frame: Through study completion, an average of 1 year.

Secondary outcomes

  1. Posttranslational modification of proteins in muscle biopsies.

    The obtained muscle samples will be subjected to mass spectrometry analysis. This measurement shows posttranslational modification that regulates protein function.

    Time frame: 5 years

Other outcomes

  1. Changes in content of metabolites in muscles and blood plasma as a result of exercise and during subsequent insulin stimulation.

    Concentration of several hundreds of metabolites in glucose, lipid and protein metabolism will be analyzed by mass spectrometry and liquid chromotography.

    Time frame: 5 years

  2. Changes in gene-expression in muscle as a result of exercise and during subsequent insulin stimulation.

    Gene-expression in muscle samples will be measured by RNA.sequencing.

    Time frame: 5 years

07

Study locations

1 site
  • Department of Exercise, Nutrition and Sports, Faculty of Sciences, University of Copenhagen
    København, 2100, Denmark
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 6, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04178603
Lead sponsor
University of Copenhagen
Collaborators
Pfizer, University of Sydney
Responsible party
Professor Jorgen FP Wojtaszewski (Professor, University of Copenhagen) — Principal investigator
First posted
Nov 26, 2019
Start date
Jul 5, 2018
Primary completion
Sep 1, 2020
Completion
Sep 1, 2020
Last update
Jan 6, 2022

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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