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.
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
- Type of treatment
- Injection or infusion, Surgery or procedure, Lifestyle or therapy programme
- 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
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- 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.
Finland1 site, 1 recruiting
- Recruiting
Turku PET Centre
Turku, 20521
Pirjo Nuutila, Professor, 35823131868, pirjo.nuutila@utu.fi
Sanna Himanen, RN, +358469200200, sanna.himanen@varha.fi
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.
- Conditions
- Obesity and Overweight
- 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 group | Role | What they receive |
|---|---|---|
| TOTAL dose test | Experimental | The 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 |
| TOTAL | Experimental | The 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.
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)
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
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
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
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.
- First posted18 Dec 2024
- Study start25 Jan 2023
- Primary completionDec 2024 (estimated)
- Study completionDec 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Obesity and OverweightStudies of the same condition, open and under way.
- More trials run by Turku University HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Turku University Hospital
- Sponsor type
- Other government
- Responsible party
- Principal investigator, Pirjo Nuutila, Turku University Hospital
- Investigators
- Lauri Nummenmaa, Professor, Principal investigator, University of TurkuPirjo Nuutila, professor, Principal investigator, University of Turku, Turku University Hospital
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
Study at a glance
From the registry record, last updated by the sponsor on 18 Dec 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Total-body Glucose Utilization in Obesity
- ClinicalTrials.gov ID
- NCT06739473
- Acronym / sponsor ID
- TOTAL / T335/2022
- Conditions
- Obesity and Overweight
- Keywords
- obesity, radiowater, PET
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Turku University HospitalOther government
- Study start
- 25 Jan 2023 (actual)
- Primary completion
- Dec 2024 (estimated)
- Study completion
- Dec 2024 (estimated)
- First posted
- 18 Dec 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Basic science
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| TOTAL dose test | Experimental | Radiation: H2[15O]O PET/CTThe 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 |
| TOTAL | Experimental | Behavioral: Movies, Behavioral: Cold, Drug: Hyperinsulinemic euglycemic clamp, Radiation: H2[15O]O PET/CT, Radiation: [18F]FDG PET/CT, Drug: CEUS or Contrast enhanced UltrasoundThe 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. |
Who may qualify
- Ages
- 20 to 60 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- 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
Key exclusion criteria (9 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| MoviesParticipants will watch eight short movie clips, and the changes different emotions evoked by the clips will be studied using H2[15O]O PET/CT. | Behavioural | TOTAL |
| ColdParticipants 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. | Behavioural | TOTAL |
| Hyperinsulinemic euglycemic clampParticipants 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. | Drug | TOTAL |
| H2[15O]O PET/CTH2[15O]O PET/CT, with a dose of 25-700 MB/bolus repeated 2-8 times per scan. | Radiation | TOTAL, TOTAL dose test |
| [18F]FDG PET/CTWhole-body [18F]FDG PET/CT scan to study tissue glucose uptake, dose 100 MBq | Radiation | TOTAL |
| CEUS or Contrast enhanced UltrasoundContrast-enhanced ultrasound of left forearm muscles is performed during fasting and after 30-40 minutes of hyperinsulinemia | Drug | TOTAL |
Primary outcome
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
Brain, liver, skeletal muscle and brain blood-flow (ml/100 g/min) measured with H2[15O]O PET/CT
4 secondary outcomes
Effects of insulin on skeletal muscle microvascular perfusion
Time frame: Change from fasting condition to 10 minutes and 50 minutes after the start of insulin infusion
Tissue insulin-stimulated glucose uptake
Time frame: Measured from 60 to 110 minutes after the start of insulin infusion
Effects of emotions on whole-body blood flow
Time frame: Measured during 60-second activation blocks (visual stimuli) or during 5 min cold-exposure
Range of effective and feasible radiowater doses with whole-body PET/CT
Time frame: During repetitive H2[15O]O scans (a total of 120 minutes)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Dec 2024.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Lauri Nummenmaa, Professor principal investigator
University of Turku
Pirjo Nuutila, professor principal investigator
University of Turku, Turku University Hospital
1 site in 1 country: see every site and its status.
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.