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The influence of amlodipine/atorvastatin single pill therapy in patients of newly diagnosed hypertension and dyslipidemia on vascular endothelial function and endothelial microparticle

The influence of amlodipine/atorvastatin single pill therapy in patients of newly diagnosed hypertension and dyslipidemia on vascular endothelial function and endothelial microparticle

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPN-15005827
Enrollment
Unknown
Registered
2015-01-10
Start date
2011-12-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

hypertension and hyperlipidemia

Interventions

1:amlodipine/atorvastatin 5mg/10mg

Sponsors

Peking university third hospital cadiology department
Lead Sponsor

Eligibility

Sex/Gender
All
Age
34 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. age 30-65 year-old male or female; 2. blood pressure between 140/90mmHg and180/110mmHg; 3. new diagnosed hypertension or hypertension history but do not have any antihypertesive drugs for the past 2 weeks; 4. hyperlipidemia history or rencent hyperlipidemia (LDL-C more than 3.37mmol/or T-CHO more than 5.18mmol/L); 5. agree to Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. secondary hypertension; 2. left ventricular dysfunction (LVEF less than 50%) or accroding NYHA heart funtion are class III-IV; 3. Active liver disease or signifcant abnomal hepatic function (ALT more than 3.0*ULN and or bilirubin more than 1.5*ULN); 4. severe chronic renal disease,Measured or estimated eGFR less than 30ml/min/1.73m2 or renal dialysis; 5. diagnosed coronary heart disease; 6. diagnosed type 1 or type 2 diabetes; 7. hemorrhagic or ischemic cerebral vascular disease; 8. pregnant or lactating women; 9. infectious diseases in the past three months; 10. tumor history; 11. autoimmune diseases; 12. various causes of bleeding disorders; 13. taking aspirin in 2 weeks; 14. with life expectancy shorter than 12 months of clinical concomitant diseases, or can not complete all follow-up; 15. known allergic to amlodipine or HMG-CoA reductase inhibitors, or had a serious adverse reaction due to taking these drugs.

Design outcomes

Primary

MeasureTime frame
microparticles;

Countries

China

Contacts

Public ContactZu lingyun
dr_zly@123.com+86 13910609953

Outcome results

None listed

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