- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03843255
Defining the Genetics, Biomarkers and Outcomes for Dilated Cardiomyopathy (Go-DCM)
Defining the Genetics, Biomarkers and Outcomes for Dilated Cardiomyopathy: a Prospective Multi-centre Observational Study
Finding new ways to diagnose and treat Dilated Cardiomyopathy (DCM) could improve the health and well-being of patients with this condition. The main aim of this research study is to help develop better ways of diagnosing and treating patients with DCM. The information that is collected may help develop tailored treatments for patients with this disease in the future. This research study will recruit patients with DCM from a number of centres across England and follow their health over a period of years. Patients will give some blood samples for a type of genetic test called whole genome sequencing (WGS) to look for genetic changes. Patients will also have a magnetic resonance imaging (MRI) scan of their heart to look for any changes in the heart such as scarring, and check their heart function. The aim of this study is to discover if using WGS and MRI can improve the diagnosis of DCM. Another aim of the study is to look at how genetic changes and scarring in the heart may affect the progress of the disease.
Studying patients with DCM may also help the investigators learn more about diagnosing and treating other diseases of the heart. The second aim of this study is to see whether using WGS and MRI scanning can also be useful in other types of heart diseases which might be affected by genetic changes or scarring in the heart.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study will recruit patients from a number of hospitals in England and study them over a number of years. The study will be divided in 2 parts. Part 1 will recruit patients with a diagnosis of DCM, Part 2 will recruit patients diagnosed with other heritable cardiovascular disorders. Family members of patients may be invited to take part in the study. Children may also be approached to take part in the study.
Patients will attend for a baseline visit for a cardiovascular magnetic resonance (CMR) scan, completion of quality of life questionnaires, collection of blood samples for whole genome sequencing and biomarker analysis, and collection of clinical data. Collection of health information via national registries including Office of National Statistics (ONS) and Hospital Episodes Statistics (HES) will be continued over the patients's lifetime. This will not require any direct contact with the participant.
Recruitment will take place over a 3 year period, with annual completion of questionnaires at patients scheduled hospital visits. If the patient is not scheduled to attend the hospital for regular follow up, then patients may complete the questionnaires via an online system or over the telephone. Patients will be asked to complete questionnaires annually for 5 years. Sub-sets of patients may be invited for additional tests including exercise testing, and stress perfusion scans. These tests will not form part of the core tests for the study, and patients may choose not to have them. Separate informed consent will be obtained from participants for any additional tests.
If patients are having clinical diagnostic tests that involve the removal of tissue, they may be asked to donate any surplus tissue sample, or be asked to provide their consent to collect an additional tissue sample. Separate informed consent will be obtained from participants for donation of additional tissue samples.
Where patients are scheduled to have a CMR scan as part of their routine clinical care, an additional CMR scan for research purposes may not be required.
Children will not be asked to complete any annual questionnaires, health information will be collected via ONS and HES.
Family members of patients who take part in the study will only be asked to donate a blood or saliva sample, and provide consent to collection of their health information via ONS and HES records. They will not have any clinical tests such as CMR.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: James Ware
- Phone Number: 0330 128 2294
- Email: go-dcm@imperial.ac.uk
Study Contact Backup
- Name: Chief Investigator
- Phone Number: 0330 128 2294
- Email: go-dcm@imperial.ac.uk
Study Locations
-
-
-
Leeds, United Kingdom, LS1 3EX
- Recruiting
- Leeds Teaching Hospitals NHS Trust
-
Contact:
- Dr John Greenwood
-
Leicester, United Kingdom, LE3 9QP
- Recruiting
- Glenfield Hospital
-
Contact:
- Prof Gerry McCann
-
Liverpool, United Kingdom, L14 3PE
- Recruiting
- Liverpool Heart and Chest Hospital NHS Foundation Trust
-
Contact:
- Dr David Wright
-
London, United Kingdom, SW3 6NP
- Recruiting
- Royal Brompton & Harefield NHS Foundation Trust
-
Contact:
- Dr Sanjay Prasad
-
Oxford, United Kingdom
- Recruiting
- Oxford University Hospitals NHS Foundation Trust
-
Contact:
- Dr Masliza Mahmod
-
Southampton, United Kingdom, SO16 6YD
- Not yet recruiting
- Southampton General Hospital
-
Contact:
- Dr Charles Peebles
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
- Patients of any age with diagnosed DCM (part 1), and
- Their family members with other heritable cardiovasacular disease (affected and unaffected), or other eligible patients with hypokinetic non-dilated cardiomyopathy (part 2)
Description
PART 1
Inclusion Criteria:
- Male or female participants of any age
- Capacity to provide informed consent
- Patients with a confirmed diagnosis of DCM
- Affected family members of patients meeting diagnostic criteria for DCM
Exclusion Criteria:
- DCM attributed to chemotoxicity (from chemotherapeutic agents, drugs of abuse)
- DCM attributed to systemic inflammatory myopathies (eg sarcoid, systemic lupus erythematosus)
- Patients who lack capacity to consent for themselves
Patients with a confirmed history of coronary artery disease, assessed using standard UK clinical practice guidelines, defined as one or more of the following:-
- >50% narrowing, any major epicardial coronary artery on invasive or computed tomography coronary angiography
- CMR suggestive of previous myocardial infarction of ≥2 segments of ≥50% infarction of the LV wall
- Previous percutaneous coronary intervention or coronary bypass surgery
- History of primary valvular heart disease or congenital heart disease
- Severe, untreated or untreatable hypertension (systolic blood pressures routinely >180 mm Hg and/or diastolic blood pressures >120 mm Hg)
PART 2
Inclusion Criteria:
- Males or females of any age
- Capacity to provide informed consent
- Patients with hypokinetic non-dilated cardiomyopathy, or
- Family members of DCM patients with possible or probable DCM or
- Patients with a confirmed diagnosis of heritable cardiovascular disease or
- Family members of patients with heritable cardiovascular disease, both affected and unaffected
Exclusion Criteria:
- Patients who lack capacity to consent for themselves
Patients with a confirmed history of coronary artery disease, assessed using standard UK clinical practice guidelines, defined as one or more of the following:-
- >50% narrowing, any major epicardial coronary artery on invasive or computed tomography coronary angiography
- CMR suggestive of previous myocardial infarction of ≥2 segments of ≥50% infarction of the LV wall
- Previous percutaneous coronary intervention or coronary bypass surgery
- History of primary valvular heart disease or congenital heart disease
- Severe, untreated or untreatable hypertension (systolic blood pressures routinely >180 mm Hg and/or diastolic blood pressures >120 mm Hg)
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Other
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Part 1: Dilated Cardiomyopathy patients
Approximately 1200 patients recruited prospectively from participating sites with a diagnosis of Dilated Cardiomyopathy (DCM).
Will also include approximately 800 retrospective patients diagnosed with DCM currently biobanked by the lead site.
|
Patients with a confirmed diagnosis of DCM will have samples that undergo whole genome sequencing and biomarker analysis
Other Names:
|
Part 2: Heritable Cardiovascular Disease
Patients may be recruited with other diagnosed heritable cardiovascular disorders.
Family members of patients may be invited to take part in the study.
Children may also be approached to take part in the study.
|
Biomarker analysis will be undertaken on samples
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The incidence of major adverse cardiovascular events over 5 years
Time Frame: 5 years
|
The incidence of major adverse cardiovascular events over 5 years,defined as:-
|
5 years
|
Incidence of novel gene variants as assessed using whole genome sequencing
Time Frame: 5 years
|
Identifying the gene variants contributing to DCM and specifically the incidence of these variants in the target population.
|
5 years
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: James Ware, Imperial College London
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 18IC4391
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- Study Protocol
- Statistical Analysis Plan (SAP)
- Informed Consent Form (ICF)
- Clinical Study Report (CSR)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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