Skip to content

Construct a predictive model for the efficacy and safety of clopidogrel Based on pharmacogenomics technology in Tibetan patients

Construct a predictive model for the efficacy and safety of clopidogrel Based on pharmacogenomics technology in Tibetan patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400092691
Enrollment
Unknown
Registered
2024-11-21
Start date
2024-11-29
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Diseases such as atherosclerosis that require the use of clopidogrel

Interventions

A group of Tibetan patients taking clopidogrel for 30 days or more:None

Sponsors

Hospital of Chengdu Office of People’s Government of Tibetan Autonomous Region (Hospital.C.T.)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Tibetan patients who have taken clopidogrel for 30 days or more as prescribed by a specialist physician; 2.Age =18 years; 3.Patients voluntarily participate in this study and have signed an informed consent form in writing;

Exclusion criteria

Exclusion criteria: 1.Patients with contraindications to antiplatelet therapy; 2.Individuals with multiple organ dysfunction syndrome (MODS); 3.Autoimmune diseases; 4.The patient refuses to participate in this study;

Design outcomes

Primary

MeasureTime frame
The primary composite endpoint (death,myocardial infarction,confirmed stent thrombosis,stroke,etc.);Bleeding event;Platelet inhibition rate;

Countries

China

Contacts

Public ContactXiaosi Li

Hospital of Chengdu Office of People’s Government of Tibetan Autonomous Region (Hospital.C.T.)

lixiaosiyyy@126.com+86 28 85537965

Outcome results

None listed

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