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The effect of the combination of antihypertensive and urate lowering therapy on vascular endothelial function in patients with hypertensive and asymptomatic hyperuricemia--A random ,open clinical trial

The effect of the combination of antihypertensive and urate lowering therapy on vascular endothelial function in patients with hypertensive and asymptomatic hyperuricemia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003965
Enrollment
Unknown
Registered
2013-11-25
Start date
2013-12-01
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 with asyptomatic hyperuricemia

Interventions

invention group:anti-hypertension, life style invention and Benzbronmarone

Sponsors

China-Japan friendship hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. participants with age between eighteen to sixty years old, male or female; 2. body mass index 420 umol/L (7 mg/dL); 5. participants must sign informed consent; 6. type of uric acid discharge poor: uric acid drainage less than 0.48 mg/kg/h, uric acid clearance (Cua, urinary uric acid * every minute urine volume/serum uric acid) < 6.2 ml/min. the Cua/Ccr ratio < 5%.

Exclusion criteria

Exclusion criteria: 1. SBP >180 MMHG; 2. DBP >110 MMHG; 3. gout; 4. uric acid type(generate too much): uric acid discharge more than 0.51 mg/kg/h, uric acid clearance rate was 6.2 ml/min.; 5. secondary hypertension; 6. a history of heart cerebrovascular disease (such as coronary heart disease, myocardial infarction, heart failure, stroke, transient ischemic attack (TIA); 7. always used diuretics and beta-blocker; 8. used promoting blood uric acid agents ago; 9. heparin (including low molecular heparin) treatment; 10. need to use anti-arrhythmia drug; 11. use drugs including diuretics and other influence uric acid; 12. use systemic corticosteroids drugs and non-steroidal anti-inflammatory drugs (NSAIDs); 13. drug abuser or drunkard; 14. pregnancy and lactation; 15. clinical trial enrolling in the past 30 days; 16. participants with some diseases are not suitable to enrolling the trial according to the researchers' judgment; 17. allergy to benzbromarone; 18. patients must use beta blockers (including ophthalmic), diureticsin after entering this test period (2 weeks follow-up); 19. with a personal or family history of psoriasis; 20. serum creatinine values was below 1.5 mg/dL, and Ccr 3 * ULN, total bilirubin > 2 * ULN).

Design outcomes

Primary

MeasureTime frame
the flow mediated dilation, FMD;Pulse wave velocity, PWV;endothelial Microparticles EM;

Secondary

MeasureTime frame
hyper- sensitivity C -reactive protein hs-CRP;urinary microalbuminuria, UMA;atherogenic index of plasma, AI;

Countries

China

Contacts

Public ContactJiao Yuan

China-Japan friendship Hospital

jiaoyuanzr@163.com+ 86 13910296895

Outcome results

None listed

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