iPSC Biobank of Biomarkers Diversity in Cardiovascular Disease

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorLondon Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

About this trial

The Investigators will create a clinical database and a Biobank of stem cells derived from the blood of participants with cardiovascular disease. The Investigators will recruit participants from diverse racial and ethnic backgrounds with equal representation from both sexes. The Investigators expect to create stem cells and analyze the blood for protein biomarkers and genetic causes of cardiovascular disease. The stem cell biobank and clinical data will be a powerful tool for studying cardiovascular disease.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adult (18 to 80 years of age)

Cardiovascular Disease (CVD)

Cerebrovascular Disease (CBD)

Peripheral Vascular Disease (PVD)

Disqualifiers

Younger than 18 years of age.

Patients not able to provide consent.

Trial population

We will recruit 200 participants including 150 patients with cardiovascular disease and 50 healthy control participants.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

200 Participants
are grouped into 2 trial groups
Group A: study controls
Group B: cardiovascular disease

Trial outcomes

Primary outcomes

1

REDCap Database

Identify patients with cardiovascular disease from ethnically diverse backgrounds and create a clinical database with REDCap.

Time frame
10 years
2

Induced pluripotent stem cell (iPSC) Biobank

Reprogram peripheral blood mononuclear cells (PBMC) to iPSCs.

Time frame
10 years
3

Differentiation into Cardiovascular lineages

Differentiate of iPSCs into different cardiovascular lineages (endothelial cells, smooth muscle cells, cardiomyocytes, etc.)

Time frame
10 years
4

Molecular profiling of participants

Molecular profiling of iPSC-derived tissue and patient serum using microarray, DNA sequencing, and high throughput "omics" technologies (transcriptomic analysis, proteomic analysis, metabolomic studies, and functional assays).

Time frame
10 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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