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Epegenomic study for different clinical type in familial hypercholesterolemia with coronary artery disease

Epegenomic study for different clinical type in familial hypercholesterolemia with coronary artery disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024074
Enrollment
Unknown
Registered
2019-06-24
Start date
2019-07-01
Completion date
Unknown
Last updated
2019-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Familial hypercholesterolemia

Interventions

gene :Methylation

Sponsors

Changzhou Wujin Peoples' Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Patients undergoing coronay angiography exmination in the department of cardiology, between June 1st 2016 and May 30 2019.

Exclusion criteria

Exclusion criteria: 1. Secondary hypercholesterolemia; 2. Absence of traditional lipid profiles; 3. Agedless than 18 years.

Design outcomes

Primary

MeasureTime frame
Methylation;—

Countries

China

Contacts

Public ContactCai Gaojun

Changzhou Wujin Peoples' Hospital

cgj982@126.com+86 13685213221

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026