Diabetes Mellitus, Type 2NCT05232812
Validation of 3-[11C]-OHB
A study testing 3-[11C]-OHB in people with Diabetes Mellitus, Type 2 and Heart Failure, run by University of Aarhus at 1 site in Denmark.
Trial summary
Ketone bodies are produced in the liver at high levels of fatty acids, and act as an important source of energy for the brain and heart during fasting. The energy production from ketone metabolism is less oxygen-demanding than both glucose and fatty acid metabolism, and ketone substances can therefore be a very… Read more about this study
- Who is it for?
- Ages 50 to 70 yearsHealthy volunteers can take part
- Conditions the study is for
- Diabetes Mellitus, Type 2, Heart Failure, Healthy
- What is being tested?
- 3-[11C]-OHB
- Type of treatment
- Pill or oral medicine, Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 6 participants
- Where
- 1 siteDenmark
- Study dates
- 1 Jun 2022to 29 Mar 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 50 to 70 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Age between 50-70 years
- BMI: 20-30 kg/m^2
Who cannot join
- All drugs that could affect the outcome
- HbA1c > 48 mmol/mol
- Known heart failure og episodes of acute myocardial infarction
- Liver disease ALAT > higher than 3 times of the normal level
- Kidney disease eGFR < 60 ml/min
- Blood donation in the last 3 months before inclusion
- Participation in other studies with radiation in the last 6 months
- Alcohol addiction
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Human Ketone Metabolism - Validation of 3-[11C]-OHB as a New PET Ketontracer
Ketone bodies are produced in the liver at high levels of fatty acids, and act as an important source of energy for the brain and heart during fasting. The energy production from ketone metabolism is less oxygen-demanding than both glucose and fatty acid metabolism, and ketone substances can therefore be a very energy-efficient substrate for the heart. Insulin-resistant people as well as people with heart disease have difficulty burning glucose in the heart due to the insulin resistant condition and are therefore dependent on other energy sources such as free fatty acids and ketones. Because ketones are oxygen-sparing compared to fatty acids, interventions that increase the level of ketone bodies can potentially reduce the heart's need for oxygen in patients with narrowed coronary arteries. PET/CT is a functional and non-invasive imaging modality and suitable for tracking the fate of metabolites non-invasively, as most substrates or metabolites can be labeled by a PET isotope.
The purpose of this experiment is therefore to validate a new ketone tracer called 3-[11C]-OHB. Implementation of the 3-[11C]-OHB tracer will in future allow the investigators to more directly estimate the impact of different levels of ketone bodies on organ functions by measuring tissue-specific ketone uptake, both after intravenous and oral administration.
Read the detailed description
Background:
Ketone bodies consists of 3-hydroxybutyrat, acetoacetate, and acetone. They are produced in the liver at high levels of fatty acids, and act as an important source of energy for the heart, brain and skeletal muscle during fasting. Energy production by ketone metabolism is less oxygen-intensive than both glucose and fatty acid metabolism, and ketone substances can therefore be a highly energy-efficient substrate. Insulin resistant individuals as well as people with heart disease have difficulty utilising glucose in the heart due to the insulin resistant condition and are therefore dependent on other energy sources such as free fatty acids and ketones. Because ketones are oxygen sparing compared to fatty acids, interventions that increase the level of ketone bodies can potentially reduce the heart's need for oxygen in patients with narrowed coronary arteries. This has led to an increased focus on the potential of ketone bodies in the treatment of a number of diseases, including especially cardiovascular disease.
Our group has shown that ketone bodies are efficiently absorbed by the heart despite maximal stimulation with insulin and glucose. In the study, healthy subjects increased the level of circulating ketone bodies to approximately 4 millimolar with a continuous ketone infusion, which resulted in a 50% reduction in cardiac glucose consumption. Since the consumption of free fatty acids in the experiment was unchanged and the overall work of the heart was the same, up to 50% of the heart's energy consumption was thus covered by ketone bodies. In addition, the high levels of ketone bodies led to a marked increase in the blood flow to the heart, which could potentially further benefit patients with narrowed coronary arteries
PET/CT is a functional and non-invasive imaging modality that is well established in oncological staging and treatment monitoring. The technique is also suitable for tracking the fate of metabolites non-invasively, as most substrates or metabolites can be labeled by a suitable PET isotope. PET has sufficient spatial and temporal resolution to enable direct quantification of e.g. uptake and oxidation rates and has been successfully used by our department to assess heart efficiency, oxygen consumption and fatty acid metabolism.
Purpose With this study, the investigators want to determine the metabolism of ketone bodies in healthy individuals and validate a newly developed ketone PET tracer for use in humans called 3-[11C]-OHB. Previous studies conducted by our and others' groups have only been able to indirectly estimate the uptake of ketone bodies into the heart. With 3-[11C]-OHB, the investigators will be able to directly measure tissue-specific ketone uptake, both after intravenous and oral administration.
Ihe investigators will apply state-of-the-science PET/CT tracer techniques and well-established models for estimating ketone metabolism (kinetics) and the radiation exposure of the tracer. Implementation of the 11C-3-OHB tracer in the future will allow the investigators to more directly estimate the impact of different levels of ketone bodies on organ functions, not least in the heart.
In this study, the investigators plan specifically
- To investigate the biodistribution and kinetics of the tracer 3-[11C]-OHB
- To estimate the radiation exposure of 3-[11C]-OHB by intravenous and oral administration of the tracer
Methods:
Six healthy and overweight (BMI: 28-40 kg/m^2) aged 50-70 years will undergo two PET/CT scans with 3-[11C]-OHB. One scan will be performed with the injection of 200 MBq of tracer and the other one will be performed with the subjects orally ingestion 100 MBq of the tracer. Following administration of the tracer, dynamic PET scans over the whole body will be performed to measure the biodistribution and radiation exposure of the tracer.
- Conditions
- Diabetes Mellitus, Type 2, Heart Failure, Healthy
- Being tested
- 3-[11C]-OHB
- Keywords
- Ketone bodies, Whole-body biodistribution
- Medical subject headings
- Diabetes Mellitus, Type 2, Heart Failure
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
3-[11C]-OHBRadiation
The PET tracer 3-[11C]-OHB is used to quantify 3-hydroxybutyrate uptake
| Study group | Role | What they receive |
|---|---|---|
| Administration of 3-[11C]-OHB | Experimental | All participants will first be injected with 200 MBq 3-[11C]-OHB followed by an oral ingestion of 100 MBq 3-[11C]-OHB. Receives: Radiation: 3-[11C]-OHB |
What is being measured
The primary outcome is the main question the study is designed to answer.
Biodistribution of 3-[11C]-OHB
The investigators will measure time activity curves by quantifying uptake of the PET ketone tracer 3-[11C]-OHB in kilo becquerel/ml over time (seconds).
Measured: Through study completion, an average of 6 months
Radiation exposure of 3-[11C]-OHB
The investigators will measure radiation exposure of 3-[11C]-OHB in millisievert in relevant organs.
Measured: Through study completion, an average of 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Feb 2022
- Study start1 Jun 2022
- Primary completion29 Mar 2023
- Study completion29 Mar 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Diabetes Mellitus, Type 2Studies of the same condition, open and under way.
- More trials run by University of AarhusThe 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 N/A
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 6 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Aarhus
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05232812
- Sponsor's protocol ID
- 1-10-72-290-20
- Status last verified
- Jan 2023
- First submitted
- 10 Jan 2022
- Last updated
- 31 Mar 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Luong TV, Nielsen EN, Falborg L, Kjaerulff MLG, Tolbod LP, Sondergaard E, Moller N, Munk OL, Gormsen LC. Intravenous and oral whole body ketone dosimetry, biodistribution, metabolite correction and kinetics studied by (R)-[1-11C]beta-hydroxybutyrate ([11C]OHB) PET in healthy humans. EJNMMI Radiopharm Chem. 2023 Jun 14;8(1):12. doi: 10.1186/s41181-023-00198-z.
PubMed 37314530
Study at a glance
From the registry record, last updated by the sponsor on 31 Mar 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Human Ketone Metabolism - Validation of 3-[11C]-OHB as a New PET Ketontracer
- ClinicalTrials.gov ID
- NCT05232812
- Acronym / sponsor ID
- 1-10-72-290-20
- Conditions
- Diabetes Mellitus, Type 2, Heart Failure, Healthy
- Keywords
- Ketone bodies, Whole-body biodistribution
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 6 participants (actual)
- Lead sponsor
- University of AarhusUniversity, hospital or other
- Study start
- 1 Jun 2022 (actual)
- Primary completion
- 29 Mar 2023 (actual)
- Study completion
- 29 Mar 2023 (actual)
- First posted
- 10 Feb 2022 (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.
Ketone bodies are produced in the liver at high levels of fatty acids, and act as an important source of energy for the brain and heart during fasting. The energy production from ketone metabolism is less oxygen-demanding than both glucose and fatty acid metabolism, and ketone substances can therefore be a very energy-efficient substrate for the heart. Insulin-resistant people as well as people with heart disease have difficulty burning glucose in the heart due to the insulin resistant condition and are therefore dependent on other energy sources such as free fatty acids and ketones. Because ketones are oxygen-sparing compared to fatty acids, interventions that increase the level of ketone bodies can potentially reduce the heart's need for oxygen in patients with narrowed coronary arteries. PET/CT is a functional and non-invasive imaging modality and suitable for tracking the fate of metabolites non-invasively, as most substrates or metabolites can be labeled by a PET isotope.
The purpose of this experiment is therefore to validate a new ketone tracer called 3-[11C]-OHB. Implementation of the 3-[11C]-OHB tracer will in future allow the investigators to more directly estimate the impact of different levels of ketone bodies on organ functions by measuring tissue-specific ketone uptake, both after intravenous and oral administration.
Detailed description
Background:
Ketone bodies consists of 3-hydroxybutyrat, acetoacetate, and acetone. They are produced in the liver at high levels of fatty acids, and act as an important source of energy for the heart, brain and skeletal muscle during fasting. Energy production by ketone metabolism is less oxygen-intensive than both glucose and fatty acid metabolism, and ketone substances can therefore be a highly energy-efficient substrate. Insulin resistant individuals as well as people with heart disease have difficulty utilising glucose in the heart due to the insulin resistant condition and are therefore dependent on other energy sources such as free fatty acids and ketones. Because ketones are oxygen sparing compared to fatty acids, interventions that increase the level of ketone bodies can potentially reduce the heart's need for oxygen in patients with narrowed coronary arteries. This has led to an increased focus on the potential of ketone bodies in the treatment of a number of diseases, including especially cardiovascular disease.
Our group has shown that ketone bodies are efficiently absorbed by the heart despite maximal stimulation with insulin and glucose. In the study, healthy subjects increased the level of circulating ketone bodies to approximately 4 millimolar with a continuous ketone infusion, which resulted in a 50% reduction in cardiac glucose consumption. Since the consumption of free fatty acids in the experiment was unchanged and the overall work of the heart was the same, up to 50% of the heart's energy consumption was thus covered by ketone bodies. In addition, the high levels of ketone bodies led to a marked increase in the blood flow to the heart, which could potentially further benefit patients with narrowed coronary arteries
PET/CT is a functional and non-invasive imaging modality that is well established in oncological staging and treatment monitoring. The technique is also suitable for tracking the fate of metabolites non-invasively, as most substrates or metabolites can be labeled by a suitable PET isotope. PET has sufficient spatial and temporal resolution to enable direct quantification of e.g. uptake and oxidation rates and has been successfully used by our department to assess heart efficiency, oxygen consumption and fatty acid metabolism.
Purpose With this study, the investigators want to determine the metabolism of ketone bodies in healthy individuals and validate a newly developed ketone PET tracer for use in humans called 3-[11C]-OHB. Previous studies conducted by our and others' groups have only been able to indirectly estimate the uptake of ketone bodies into the heart. With 3-[11C]-OHB, the investigators will be able to directly measure tissue-specific ketone uptake, both after intravenous and oral administration.
Ihe investigators will apply state-of-the-science PET/CT tracer techniques and well-established models for estimating ketone metabolism (kinetics) and the radiation exposure of the tracer. Implementation of the 11C-3-OHB tracer in the future will allow the investigators to more directly estimate the impact of different levels of ketone bodies on organ functions, not least in the heart.
In this study, the investigators plan specifically
- To investigate the biodistribution and kinetics of the tracer 3-[11C]-OHB
- To estimate the radiation exposure of 3-[11C]-OHB by intravenous and oral administration of the tracer
Methods:
Six healthy and overweight (BMI: 28-40 kg/m^2) aged 50-70 years will undergo two PET/CT scans with 3-[11C]-OHB. One scan will be performed with the injection of 200 MBq of tracer and the other one will be performed with the subjects orally ingestion 100 MBq of the tracer. Following administration of the tracer, dynamic PET scans over the whole body will be performed to measure the biodistribution and radiation exposure of the tracer.
Study design
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Administration of 3-[11C]-OHB | Experimental | Radiation: 3-[11C]-OHBAll participants will first be injected with 200 MBq 3-[11C]-OHB followed by an oral ingestion of 100 MBq 3-[11C]-OHB. |
Who may qualify
- Ages
- 50 to 70 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Age between 50-70 years
- BMI: 20-30 kg/m^2
Key exclusion criteria (8 listed)
- All drugs that could affect the outcome
- HbA1c > 48 mmol/mol
- Known heart failure og episodes of acute myocardial infarction
- Liver disease ALAT > higher than 3 times of the normal level
- Kidney disease eGFR < 60 ml/min
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 |
|---|---|---|
| 3-[11C]-OHBThe PET tracer 3-[11C]-OHB is used to quantify 3-hydroxybutyrate uptake | Radiation | Administration of 3-[11C]-OHB |
Primary outcome
Biodistribution of 3-[11C]-OHB
Time frame: Through study completion, an average of 6 months
The investigators will measure time activity curves by quantifying uptake of the PET ketone tracer 3-[11C]-OHB in kilo becquerel/ml over time (seconds).
Radiation exposure of 3-[11C]-OHB
Time frame: Through study completion, an average of 6 months
The investigators will measure radiation exposure of 3-[11C]-OHB in millisievert in relevant organs.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Mar 2023.
- Derived from this study: PubMed 37314530Luong TV, Nielsen EN, Falborg L, Kjaerulff MLG, Tolbod LP, Sondergaard E, Moller N, Munk OL, Gormsen LC. Intravenous and oral whole body ketone dosimetry, biodistribution, metabolite correction and kinetics studied by (R)-[1-11C]beta-hydroxybutyrate ([11C]OHB) PET in healthy humans. EJNMMI Radiopharm Chem. 2023 Jun 14;8(1):12. doi: 10.1186/s41181-023-00198-z.
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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. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing 3-[11C]-OHB in people with Diabetes Mellitus, Type 2 and Heart Failure, run by University of Aarhus at 1 site in Denmark.
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 2 inclusion and 8 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: finished, as of the sponsor's last update on 31 Mar 2023. 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 Denmark. 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.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Biodistribution of 3-[11C]-OHB (time frame: Through study completion, an average of 6 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05232812, which also lists 1 linked publication.
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 31 Mar 2023.