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Obesity and OverweightPhase 4TOTALNCT06739473

Total-body Glucose Utilization in Obesity

A Phase 4 study testing Movies, Cold and Hyperinsulinemic euglycemic clamp in people with Obesity and Overweight, run by Turku University Hospital at 1 site in Finland.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

There are three goals for this study. One is to investigate how different emotions and exposure to cold affect blood flow in the body. The second aim is to study how insulin affects blood flow and tissue glucose uptake, and to study whether this effect is altered in obesity. Read more about this study

Who is it for?
Ages 20 to 60 yearsHealthy volunteers can take part
Conditions the study is for
Obesity and Overweight
What is being tested?
Movies, Cold and Hyperinsulinemic euglycemic clamp
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteFinland
Study dates
25 Jan 2023to Dec 2024
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 60 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Age 20-60 years
  • BMI either 18.5-25 kg/m2 or above 30 kg/m2
  • Use of hormonal contraception for women in child bearing age

Who cannot join

  • In the lean group history of obesity or type 2 diabetes
  • In the group with obesity: current or previous use of GLP-1-agonists or insulin
  • History of eating disorders
  • Smoking, use of narcotics, excessive use of alcohol
  • Previous participation in PET studies
  • Previous significant exposure to radiation
Show all 9Show fewer
  • Claustrophobia
  • Active plans for concieving (both sexes)
  • Any other condition that in the opinion of the investigator could create a hazard to the subject safety, endanger the study procedures or interfere with the interpretation of study results

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Aino Latva-Rasku, MD, PhD contact

358+23139857

aehyyp@utu.fi

Sanna Himanen, RN contact

358+469200200

sanna.himanen@varha.fi

Finland1 site, 1 recruiting
  • Turku PET Centre

    Turku, 20521

    Pirjo Nuutila, Professor, 35823131868, pirjo.nuutila@utu.fi

    Sanna Himanen, RN, +358469200200, sanna.himanen@varha.fi

    Recruiting

Other trials in Finland

About this study

There are three goals for this study. One is to investigate how different emotions and exposure to cold affect blood flow in the body. The second aim is to study how insulin affects blood flow and tissue glucose uptake, and to study whether this effect is altered in obesity. Last, the study focuses on establishing the lowest dose of a PET radiotracer, oxygen-15 labelled water, that can be used in clinical studies with a new whole-body PET scanner.

Read the detailed description

The study consists of two separate parts: the dose escalation study and the part studying the effects of emotions and insulin on blood flow.

All participants will first undergo a screening visit starting with signing an informed consent form. Then they will undergo a physical examination, are interviewed about their medical history. Finally, some routine laboratory tests are collected, and a 75 g oral glucose tolerance test is performed. The participants who are eligibile for the study will continue to the PET studies.

The dose escalation study will be completed first. In this 8 participants will be studied once with Siemens Biovision Quadra PET/CT scanner. They will receive eight doses of oxygen-15 labelledradiowater (H2[15O]O) ranging from 25 to 700 MBq, with each dose repeated twice to evaluate repeatability of each dose. These participants will not undergo any further studies.

For the other subjects, there will be two more PET study visits.

On the first visit, the effects of emotions, evoked by short movie clips or cold exposure of one leg, on whole-body blood flow will studied with oxygen-15 labelled radiowater. Each participant will be studied 8 times in one session, with repeated H2[15O]O boluses of 400 MBq followed by 7.5 min dynamic PET scans with Siemens Biovision Quadra PET/CT scanner and a 5 min recovery and wash-out period.

On the other visit the effects of insulin on circulation will be studied by performing a hyperinsulinemic, euglycemic clamp during the PET scan. During the clamp, fast-acting insulin (NovoRapid, NovoNordisk) is administered intravenously at a fixed rate (40 mU/m2 body surface area/min). Plasma glucose is monitored every 5-10 minutes, and 20 % glucose is administered at a varying rate to maintain euglycemia (5.0 mmol/L).

At the scanner a fasting H2[15O]O PET/CT scan (400 MBq) will be performed first. After this, the hyperinsulinemic, euglycemic clamp is started, and the radiowater scans are repeated 10 minutes and 50 minutes into the insulin infusion. 60 minutes after the start of clamp, 100 MBq of glucose analogue tracer [18F]fluorodeoxyglucose is administered and a 50 min dynamic PET scan is started. After the scan, insulin infusion is discontinued and participants are monitored until plasma glucose levels are adequate for safe discharge.

For a subgroup of participants, skeletal muscle microvascular bloodflow will also be assessed with contrast-enhanced ultrasound performed during fasting and 30 minutes after the start of clamp. The participants will be administered intravenous contrast agent, and after steady plasma concentration is reached (2.5 min), the contrast agent micro bubbles are destroyed with a high-intensity ultrasound signal, and the rate at which small arterioles are refilled is measured.

Data will be analysed using in-house developed programs. Regions of interest will be drawn manually for peripheral tissues (skeletal muscle, visceral, brown and subcutaneous adipose tissue, liver, kidney, intestines) and using automated segmentation tools for the brain.

Being tested
Movies, Cold, Hyperinsulinemic euglycemic clamp, H2[15O]O PET/CT, [18F]FDG PET/CT
Keywords
obesity, radiowater, PET
Medical subject headings
Obesity, Overweight

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • MoviesBehavioural

    Participants will watch eight short movie clips, and the changes different emotions evoked by the clips will be studied using H2[15O]O PET/CT.

  • ColdBehavioural

    Participants will be studied with H2[15O]O PET/CT while one of their legs will be exposed to cold to study the effects of cold stimulus on whole-body blood flow.

  • Hyperinsulinemic euglycemic clampDrug

    Participants will be administered intravenous fast acting insulin (NovoRapid, Novo Nordisk, 1 mU/m2 body surface area/min) together with 20 % glucose to maintain normal glucose values (5.0 mmol/L) to study the effects of insulin on whole body blood flow with H2[15O]O PET/CT, and to assess tissue insulin-stimulated glucose uptake with [18F]FDG PET/CT.

  • H2[15O]O PET/CTRadiation

    H2[15O]O PET/CT, with a dose of 25-700 MB/bolus repeated 2-8 times per scan.

  • [18F]FDG PET/CTRadiation

    Whole-body [18F]FDG PET/CT scan to study tissue glucose uptake, dose 100 MBq

  • CEUS or Contrast enhanced UltrasoundDrug

    Contrast-enhanced ultrasound of left forearm muscles is performed during fasting and after 30-40 minutes of hyperinsulinemia

Study groups in NCT06739473
Study groupRoleWhat they receive
TOTAL dose testExperimentalThe aim of the studies performed in this arm (8 subjects) is to test the lowest dose of H2[15O]O (radiowater) for the Siemens Quadra PET/CT scanner. Each participant will be studied once with the scanner with 4 different doses (25-700 MBq) of H2[15O]O, each repeated 2 times
Receives: Radiation: H2[15O]O PET/CT
TOTALExperimentalThe participants in this arm will undergo two PET visits. On one visit the effects of visual stimuli or cold on whole body perfusion will be studied with H2[15O]O PET/CT. On the second visit whole-body insulin sensitivity is studied with [18F]fluorodeoxyglucose PET/CT, and the acute and delayed effects of intravenous insulin on blood flow will be studied with H2[15O]O PET/CT.
Receives: Behavioral: Movies; Behavioral: Cold; Drug: Hyperinsulinemic euglycemic clamp; Radiation: H2[15O]O PET/CT; Radiation: [18F]FDG PET/CT; Drug: CEUS or Contrast enhanced Ultrasound

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Insulin-induced change in tissue blood flow

    Brain, liver, skeletal muscle and brain blood-flow (ml/100 g/min) measured with H2[15O]O PET/CT

    Measured: Change from fasting condition to 10 minutes and 50 minutes after the start of insulin infusion

Secondary outcomes (4)
  1. Effects of insulin on skeletal muscle microvascular perfusion

    The difference in the rate of refill of skeletal muscle small capillaries measured as contrast agent wash-in using contrast-enhanced ultrasound during fasting and during hyperinsulinemic, euglycemic clamp

    Measured: Change from fasting condition to 10 minutes and 50 minutes after the start of insulin infusion

  2. Tissue insulin-stimulated glucose uptake

    Skeletal muscle, adipose tissue, liver and brain glucose uptake (micromol/100g/min) during hyperinsulinemic, euglycemic clamp measured with [18F]FDG PET/CT

    Measured: Measured from 60 to 110 minutes after the start of insulin infusion

  3. Effects of emotions on whole-body blood flow

    Distribution of whole-body blood flow after visual stimuluses or cold exposure

    Measured: Measured during 60-second activation blocks (visual stimuli) or during 5 min cold-exposure

  4. Range of effective and feasible radiowater doses with whole-body PET/CT

    Repeatability and reliability of different doses of H2[15O]O in assessing tissue blood flow in the brain, skeletal muscle, myocardium, liver and adipose tissue

    Measured: During repetitive H2[15O]O scans (a total of 120 minutes)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Dec 2024
  2. Study start25 Jan 2023
  3. Primary completionDec 2024 (estimated)
  4. Study completionDec 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Basic science
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06739473
Sponsor's protocol ID
T335/2022
Acronym
TOTAL
Status last verified
Dec 2024
First submitted
29 Sep 2024
Last updated
18 Dec 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Movies, Cold and Hyperinsulinemic euglycemic clamp in people with Obesity and Overweight, run by Turku University Hospital at 1 site in Finland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 18 Dec 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Finland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Aino Latva-Rasku, MD, PhD (358+23139857, aehyyp@utu.fi), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Insulin-induced change in tissue blood flow (time frame: Change from fasting condition to 10 minutes and 50 minutes after the start of insulin infusion). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Dec 2024.

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