DiabetesDD2plaqueNCT03022344
DD2-Coronary Plaque Morphology and Plaque Progression
A study testing Cardiac CT in people with Diabetes and Plaque, run by Esbjerg Hospital - University Hospital of Southern Denmark at 1 site in Denmark.
Trial summary
However, there is only very sparse information regarding the atherosclerotic burden and cardiovascular biomarkers in the early stages of type-2 diabetes, as the vast majority of studies have concerned diabetes populations with more than 5 years average diabetes age or high-risk subgroups, who at inclusion already had… Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Diabetes, Plaque, Atherosclerosis
- What is being tested?
- Cardiac CT
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 200 participants
- Where
- 1 siteDenmark
- Study dates
- Nov 2014to Oct 2021
- 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 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Newly diagnosed (< 1 year) diabetes patients clinically classified as type-2 diabetes patients of both sex.
- Age 18 +.
Who cannot join
- Type 1 diabetes (or have age<30 years and C-peptid<300pmol/l and GAD-ab titer> 20 IU/ml).
- Renal insufficiency (GFR < 45 or se-creatinine >140 micromol/l).
- BMI > 35.
- Atrial fibrillation.
- Life expectancy below 2 years.
- Mental disease and/or misuse of alcohol or drugs that affects patient's ability to give informed consent.
- Pregnancy at time of or planned at inclusion.
- Patients with a history of prior atherothrombotic disease (including acute coronary syndromes, prior revascularization, ischemic stroke or peripheral arterial disease).
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Coronary Plaque Morphology and Plaque Progression in Patients With Newly Diagnosed Type-2 Diabetes Mellitus
However, there is only very sparse information regarding the atherosclerotic burden and cardiovascular biomarkers in the early stages of type-2 diabetes, as the vast majority of studies have concerned diabetes populations with more than 5 years average diabetes age or high-risk subgroups, who at inclusion already had atherosclerotic disease manifestations.
Consequently, this study aims on evaluating the occurrence of early-stage subclinical atherosclerosis in newly diagnosed type-2 diabetes with special emphasis on coronary plaque characteristics by modern imaging techniques. These findings will be compared to the functional status of various peripheral arterial segments and biomarkers in the cross-sectional part of this study. The 5-year follow-up study intends to describe relationships between these selected measures for general atherosclerotic involvement and the progression of the coronary atherosclerotic burden by contemporary techniques.
Read the detailed description
THE AIM
The objective of this study is to:
Study I: Compare the prevalence and complexity of coronary plaques in patients with newly discovered type-2 diabetes with a healthy control group matched for age and gender, as evaluated by coronary computed tomography angiography.
Study II: Describe the relationship between morphological, functional and biochemical estimates of arteriosclerosis in newly diagnosed type-2 diabetes.
Study III: Characterize the progression of coronary plaques in patients with newly discovered type-2 diabetes in a 5-year follow-up study.
DESIGN
"Coronary plaque morphology and plaque progression in patients with newly diagnosed type-2 diabetes mellitus" (DD2-plaque study) is a prospective cohort follow up study.
The inclusion phase will run for 2 years. The follow-up phase is 5 years from inclusion.
The DD2-plaque study (diabetic patient's cohort):
Recruitment in this cohort will take place in three ways:
- From the "Danish centers for strategic research in type 2 diabetes" (DD2) - patients who agreed to be contacted for participation in a future study.
- Direct from outpatient clinics in The Region of Southern. Patients will either be recruited through general practitioners or from outpatient clinics in The Region of Southern Denmark. The investigators expect to be able to include 100 asymptomatic patients with newly diagnosed type-2 diabetes.
Inclusion criteria
- Newly diagnosed (< 1 year) diabetes patients clinically classified as type-2 diabetes patients of both sex.
- Age 18 +.
Exclusion criteria
- Type 1 diabetes (or have age<30 years and C-peptid<300pmol/l and GAD-ab titer> 20 IU/ml).
- Renal insufficiency (GFR < 45 or se-creatinine >140 micromol/l).
- BMI > 35 kg/m2
- Atrial fibrillation.
- Life expectancy below 2 years.
- Mental disease and/or misuse of alcohol or drugs that affects patient's ability to give informed consent.
- Pregnancy at time of or planned at inclusion.
- Patients with a history of prior atherothrombotic disease (including acute coronary syndromes, prior revascularization, ischemic stroke or peripheral arterial disease).
The DD2-plaque study (control patients cohort):
100 controls will be recruited from the general population by advertisement in the local press. Controls with cardiovascular disease (criteria consistent with those described for patients with type-2 diabetes) and type-2 diabetes (undiagnosed type-2 diabetes in this group was excluded by fasting plasma glucose and by an oral glucose tolerance test) will be excluded. In addition, exclusion criteria are also consistent with those described for patients with type-2 diabetes.
Longitudinal measurements will be done at the screening visit and after 5 years.
- The proxy statement.
- Participants will fill in a questionnaire concerning:
- Cardiovascular and diabetes hereditary
- Medication
- Alcohol and drugs consumption
- Smoking habits (current, prior and never smokers)
- Family history (cardiac events or strokes for women < 65 years of age and men < 55 years of age in first generation relatives)
- Medical history
- Physical examination will include measurement of:
- Height, weight, BMI.
- Waist/hip ratio
- ECG
- Brachial blood pressure will be measured by oscillometric technics during 24 hours using TM-2430 (A\&D CO., LTD, Saitama, Japan) or BDM Mobil-O-Graph® NG Classic (IEM GmbH, Stolberg, Germany).
- Blood samples: Procedures for handling and shipping samples is available in the trial master and at www.DD2.nu under "blodprøvetagning". An exception to these procedures are that the blood samples will be frozen at site and send on ice to the biobank. 2 x 9 ml. containers with green lid (Li-hep) 2 x 2.7 ml. containers with blue lid (Na-citrat) 2 x 9 ml. containers with purple lid (EDTA) 2 x 4 ml. containers with purple/dark purple lid (EDTA) 2 x 3 ml. containers with pink lid (Fluoridcitrat) 2 x 9 ml. containers with brown lid (Serum) 1 container for urine with yellow lid 10 ml of morning midstream urine will be sampled. Urine sticks will be used to rule out urinary tract infection. If this is present the urine should be resembled. A total of 73.4 ml + 10 ml of blood will be drawn. For a subset of patients the DD2 cohort registration and the baseline visit will take place in the same day. These patients will have 146.8 ml of blood drawn on the same day. Containers will be sent to the patients.
- Biochemical analysis: total cholesterol, S-LDL-cholesterol, S-HDL-cholesterol and S-triglycerides, HbA1c, glucose, C-reactive protein, D-dimer, creatinin and fibrinogen. All analyses are performed at our local Dept. of Clinical Biochemistry.
- All patients will undergone: Carotid intima media thickness (IMT) will be measured by B-mode ultrasound (Model IE33, Koninklijke Philips Electronics N.V, Eindhoven, The Netherlands) using a linear array transducer, L11-3 with a frequency up to 11 MHz.
- Pulse wave velocity: Using sphygmocor (ArtCor, Sydney, Australia).
- Ankle brachial index.
- Albumin creatinine ratio
- Coronary atherosclerosis is evaluated by measurement of calcium in the coronary arteries and by evaluation of coronary plaques using contrast enhanced cardiac CT. Coronary artery calcifications will be estimated by the Agatston score while the evaluation of coronary plaques will be performed by a dedicated plaque-analysis tool, Auto-Plaque.
STATISTICS
Sample size estimations are performed for comparison of calcium scoring between patients with type-2 diabetes and normal controls (Un-paired evaluation) and comparison of calcium scoring between type-2 diabetes patients at inclusion and at follow-up (Paired). From previous studies on calcium scoring in the Danish Risk Score Study cohort, the standard deviation, SD, on coronary calcification is known to be 32.7 UE (Agatston Score). It is supposed that SD in the diabetic patients is equal to the figure in controls. Under the assumptions that 15% will drop-out, a MIREDIF of 20 (twice the threshold for registering the occurrence of coronary calcification in the central West Danish Heart Registry, VDH), beta= 0, 1 and alfa= 0.02 (Planned comparative analysis of 2-3 plaque-components) it is calculated, that it is needed to include 41 patients in each group for the un-paired analyses and to follow 41 diabetic patients for 5 years (Paired analysis). It is supposed, that app. 40% of type-2 diabetes patients meet the age criteria (55+/-5 years or 65+/-5 years) for comparison with the background population, which means that app. 100 type-2 diabetes patients should be included in the DD2 plaque study.
Students T-test will be used for comparison of normally distributed continuous variables and the Mann-Whitney test will be used for comparison of continuous variables that are not normally distributed. The χ2- test is performed for comparison of dichotomous variables. Continuous variables are presented as either mean or standard deviation or median and interquartile range. P-values <0.05 will be considered statistically significant. Stepwise multivariate logistic regression will be performed for analysis of which factors are associated with coronary atherosclerosis using either presence coronary artery calcification or other plaque variables as dependant variables.
- Conditions
- Diabetes, Plaque, Atherosclerosis
- Being tested
- Cardiac CT
- Keywords
- DD2 plaque study, Coronary plaque, Type-2 diabetes mellitus
- Medical subject headings
- Diabetes Mellitus, Plaque, Amyloid, Atherosclerosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Cardiac CTRadiation
| Study group | Role | What they receive |
|---|---|---|
| Healthy | Sham comparator | Patients in this cohort consist of 100 healthy patients Receives: Radiation: Cardiac CT |
| Diabetes mellitus | Sham comparator | Newly diagnosed (< 1 year) diabetes patients clinically classified as type-2 diabetes patients of both sex Receives: Radiation: Cardiac CT |
What is being measured
The primary outcome is the main question the study is designed to answer.
Progression of contrast enhanced cardiac CT in relation to baseline and follow-up cardiovascular risk factors and biomarkers.
Coronary artery calcification were quantified by non-contrast cardiac CT and were assessed by summing up the scores from all foci in the coronary arteries, expressed in Agatston units (U), using dedicated software (Syngo Calcium scoring, (Siemens Healthcare).
Measured: 5 years
Secondary outcomes (6)
Biochemical analysis in relation to contrast enhanced cardiac CT
no. of participants with abnormal laboratory values compared to abnormal/normal enhanced cardiac CT
Measured: 1 year
Body mass index (kg/m2)
Cardiovascular risk factors. No of participants with body mass index > 30 kg/m2
Measured: 1 year
Carotid intima media thickness
A measure of the combined thickness of intima and media layers of carotid artery, assessed by B-mode ultrasound.values between 0.6 and 0.7 mm have been considered normal. Values > 1 mm or more has been associated with significant increased absolute risk of atherosclerosis. No of participants with values > 1 mm.
Measured: 1 year
Ankle brachial index
An ankle brachial index between and including 0.9 and 1.2 considered normal (free from significant peripheral artery disease), while a lesser than 0.9 indicates arterial disease. No of participants with value < 0.9.
Measured: 1year
waist hip ratio (m)
Abdominal obesity was defined as a waist-hip ratioabove 0.90 for males and above 0.85 for females,or a body mass index above 30.0 kg/m2. No of participants with abdominal obesity
Measured: 1 year
Blood pressure (mmHg)
Hypertension was defined as blood pressures ≥ 140/90. No of participants with hypertension
Measured: 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Jan 2017 (estimated)
- Study startNov 2014
- Primary completionJun 2021 (estimated)
- Study completionOct 2021 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for DiabetesStudies of the same condition, open and under way.
- 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
- Screening
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Esbjerg Hospital - University Hospital of Southern Denmark
- Sponsor type
- University, hospital or other
- Collaborators
- Novo Nordisk Foundation, University of Southern Denmark, Department of Regional Health Research - Center Southwest, Edith and Vagn Hedegaard Jensens Foundation, Karola Jørgensens Foundation and Foundation for Cardiology in Southwest Denmark.
- Responsible party
- Principal investigator, Monija Mrgan, Esbjerg Hospital - University Hospital of Southern Denmark
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03022344
- Sponsor's protocol ID
- 44110
- Acronym
- DD2plaque
- Status last verified
- May 2018
- First submitted
- 9 Jan 2017
- Last updated
- 8 May 2018
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 8 May 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Coronary Plaque Morphology and Plaque Progression in Patients With Newly Diagnosed Type-2 Diabetes Mellitus
- ClinicalTrials.gov ID
- NCT03022344
- Acronym / sponsor ID
- DD2plaque / 44110
- Conditions
- Diabetes, Plaque, Atherosclerosis
- Keywords
- DD2 plaque study, Coronary plaque, Type-2 diabetes mellitus
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- Esbjerg Hospital - University Hospital of Southern DenmarkUniversity, hospital or other
- Collaborators
- Novo Nordisk Foundation, University of Southern Denmark, Department of Regional Health Research - Center Southwest, Edith and Vagn Hedegaard Jensens Foundation, Karola Jørgensens Foundation and Foundation for Cardiology in Southwest Denmark.
- Study start
- Nov 2014
- Primary completion
- Jun 2021 (estimated)
- Study completion
- Oct 2021 (estimated)
- First posted
- 16 Jan 2017 (estimated)
- 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.
However, there is only very sparse information regarding the atherosclerotic burden and cardiovascular biomarkers in the early stages of type-2 diabetes, as the vast majority of studies have concerned diabetes populations with more than 5 years average diabetes age or high-risk subgroups, who at inclusion already had atherosclerotic disease manifestations.
Consequently, this study aims on evaluating the occurrence of early-stage subclinical atherosclerosis in newly diagnosed type-2 diabetes with special emphasis on coronary plaque characteristics by modern imaging techniques. These findings will be compared to the functional status of various peripheral arterial segments and biomarkers in the cross-sectional part of this study. The 5-year follow-up study intends to describe relationships between these selected measures for general atherosclerotic involvement and the progression of the coronary atherosclerotic burden by contemporary techniques.
Detailed description
THE AIM
The objective of this study is to:
Study I: Compare the prevalence and complexity of coronary plaques in patients with newly discovered type-2 diabetes with a healthy control group matched for age and gender, as evaluated by coronary computed tomography angiography.
Study II: Describe the relationship between morphological, functional and biochemical estimates of arteriosclerosis in newly diagnosed type-2 diabetes.
Study III: Characterize the progression of coronary plaques in patients with newly discovered type-2 diabetes in a 5-year follow-up study.
DESIGN
"Coronary plaque morphology and plaque progression in patients with newly diagnosed type-2 diabetes mellitus" (DD2-plaque study) is a prospective cohort follow up study.
The inclusion phase will run for 2 years. The follow-up phase is 5 years from inclusion.
The DD2-plaque study (diabetic patient's cohort):
Recruitment in this cohort will take place in three ways:
- From the "Danish centers for strategic research in type 2 diabetes" (DD2) - patients who agreed to be contacted for participation in a future study.
- Direct from outpatient clinics in The Region of Southern. Patients will either be recruited through general practitioners or from outpatient clinics in The Region of Southern Denmark. The investigators expect to be able to include 100 asymptomatic patients with newly diagnosed type-2 diabetes.
Inclusion criteria
- Newly diagnosed (< 1 year) diabetes patients clinically classified as type-2 diabetes patients of both sex.
- Age 18 +.
Exclusion criteria
- Type 1 diabetes (or have age<30 years and C-peptid<300pmol/l and GAD-ab titer> 20 IU/ml).
- Renal insufficiency (GFR < 45 or se-creatinine >140 micromol/l).
- BMI > 35 kg/m2
- Atrial fibrillation.
- Life expectancy below 2 years.
- Mental disease and/or misuse of alcohol or drugs that affects patient's ability to give informed consent.
- Pregnancy at time of or planned at inclusion.
- Patients with a history of prior atherothrombotic disease (including acute coronary syndromes, prior revascularization, ischemic stroke or peripheral arterial disease).
The DD2-plaque study (control patients cohort):
100 controls will be recruited from the general population by advertisement in the local press. Controls with cardiovascular disease (criteria consistent with those described for patients with type-2 diabetes) and type-2 diabetes (undiagnosed type-2 diabetes in this group was excluded by fasting plasma glucose and by an oral glucose tolerance test) will be excluded. In addition, exclusion criteria are also consistent with those described for patients with type-2 diabetes.
Longitudinal measurements will be done at the screening visit and after 5 years.
- The proxy statement.
- Participants will fill in a questionnaire concerning:
- Cardiovascular and diabetes hereditary
- Medication
- Alcohol and drugs consumption
- Smoking habits (current, prior and never smokers)
- Family history (cardiac events or strokes for women < 65 years of age and men < 55 years of age in first generation relatives)
- Medical history
- Physical examination will include measurement of:
- Height, weight, BMI.
- Waist/hip ratio
- ECG
- Brachial blood pressure will be measured by oscillometric technics during 24 hours using TM-2430 (A\&D CO., LTD, Saitama, Japan) or BDM Mobil-O-Graph® NG Classic (IEM GmbH, Stolberg, Germany).
- Blood samples: Procedures for handling and shipping samples is available in the trial master and at www.DD2.nu under "blodprøvetagning". An exception to these procedures are that the blood samples will be frozen at site and send on ice to the biobank. 2 x 9 ml. containers with green lid (Li-hep) 2 x 2.7 ml. containers with blue lid (Na-citrat) 2 x 9 ml. containers with purple lid (EDTA) 2 x 4 ml. containers with purple/dark purple lid (EDTA) 2 x 3 ml. containers with pink lid (Fluoridcitrat) 2 x 9 ml. containers with brown lid (Serum) 1 container for urine with yellow lid 10 ml of morning midstream urine will be sampled. Urine sticks will be used to rule out urinary tract infection. If this is present the urine should be resembled. A total of 73.4 ml + 10 ml of blood will be drawn. For a subset of patients the DD2 cohort registration and the baseline visit will take place in the same day. These patients will have 146.8 ml of blood drawn on the same day. Containers will be sent to the patients.
- Biochemical analysis: total cholesterol, S-LDL-cholesterol, S-HDL-cholesterol and S-triglycerides, HbA1c, glucose, C-reactive protein, D-dimer, creatinin and fibrinogen. All analyses are performed at our local Dept. of Clinical Biochemistry.
- All patients will undergone: Carotid intima media thickness (IMT) will be measured by B-mode ultrasound (Model IE33, Koninklijke Philips Electronics N.V, Eindhoven, The Netherlands) using a linear array transducer, L11-3 with a frequency up to 11 MHz.
- Pulse wave velocity: Using sphygmocor (ArtCor, Sydney, Australia).
- Ankle brachial index.
- Albumin creatinine ratio
- Coronary atherosclerosis is evaluated by measurement of calcium in the coronary arteries and by evaluation of coronary plaques using contrast enhanced cardiac CT. Coronary artery calcifications will be estimated by the Agatston score while the evaluation of coronary plaques will be performed by a dedicated plaque-analysis tool, Auto-Plaque.
STATISTICS
Sample size estimations are performed for comparison of calcium scoring between patients with type-2 diabetes and normal controls (Un-paired evaluation) and comparison of calcium scoring between type-2 diabetes patients at inclusion and at follow-up (Paired). From previous studies on calcium scoring in the Danish Risk Score Study cohort, the standard deviation, SD, on coronary calcification is known to be 32.7 UE (Agatston Score). It is supposed that SD in the diabetic patients is equal to the figure in controls. Under the assumptions that 15% will drop-out, a MIREDIF of 20 (twice the threshold for registering the occurrence of coronary calcification in the central West Danish Heart Registry, VDH), beta= 0, 1 and alfa= 0.02 (Planned comparative analysis of 2-3 plaque-components) it is calculated, that it is needed to include 41 patients in each group for the un-paired analyses and to follow 41 diabetic patients for 5 years (Paired analysis). It is supposed, that app. 40% of type-2 diabetes patients meet the age criteria (55+/-5 years or 65+/-5 years) for comparison with the background population, which means that app. 100 type-2 diabetes patients should be included in the DD2 plaque study.
Students T-test will be used for comparison of normally distributed continuous variables and the Mann-Whitney test will be used for comparison of continuous variables that are not normally distributed. The χ2- test is performed for comparison of dichotomous variables. Continuous variables are presented as either mean or standard deviation or median and interquartile range. P-values <0.05 will be considered statistically significant. Stepwise multivariate logistic regression will be performed for analysis of which factors are associated with coronary atherosclerosis using either presence coronary artery calcification or other plaque variables as dependant variables.
Study design
- Primary purpose
- Screening
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Healthy | Sham comparator | Radiation: Cardiac CTPatients in this cohort consist of 100 healthy patients |
| Diabetes mellitus | Sham comparator | Radiation: Cardiac CTNewly diagnosed (< 1 year) diabetes patients clinically classified as type-2 diabetes patients of both sex |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Newly diagnosed (< 1 year) diabetes patients clinically classified as type-2 diabetes patients of both sex.
- Age 18 +.
Key exclusion criteria (8 listed)
- Type 1 diabetes (or have age<30 years and C-peptid<300pmol/l and GAD-ab titer> 20 IU/ml).
- Renal insufficiency (GFR < 45 or se-creatinine >140 micromol/l).
- BMI > 35.
- Atrial fibrillation.
- Life expectancy below 2 years.
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 |
|---|---|---|
| Cardiac CT | Radiation | Diabetes mellitus, Healthy |
Primary outcome
Progression of contrast enhanced cardiac CT in relation to baseline and follow-up cardiovascular risk factors and biomarkers.
Time frame: 5 years
Coronary artery calcification were quantified by non-contrast cardiac CT and were assessed by summing up the scores from all foci in the coronary arteries, expressed in Agatston units (U), using dedicated software (Syngo Calcium scoring, (Siemens Healthcare).
6 secondary outcomes
Biochemical analysis in relation to contrast enhanced cardiac CT
Time frame: 1 year
Body mass index (kg/m2)
Time frame: 1 year
Carotid intima media thickness
Time frame: 1 year
Ankle brachial index
Time frame: 1year
waist hip ratio (m)
Time frame: 1 year
Blood pressure (mmHg)
Time frame: 1 year
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 May 2018.
- 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. 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 Cardiac CT in people with Diabetes and Plaque, run by Esbjerg Hospital - University Hospital of Southern Denmark 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: status not confirmed, as of the sponsor's last update on 8 May 2018. 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. Some participants in this study may receive a placebo. 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?
Results are not available in the source record.
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?
Progression of contrast enhanced cardiac CT in relation to baseline and follow-up cardiovascular risk factors and biomarkers. (time frame: 5 years). 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 8 May 2018.