Skip to content

Effect of early urate-lowering therapy on artery stiffness in hypertensive patients with asymptomatic hyperuriacemia: A random, open clinical trial

Effect of early urate-lowering therapy on artery stiffness in hypertensive patients with asymptomatic hyperuriacemia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003092
Enrollment
Unknown
Registered
2013-03-05
Start date
2013-03-01
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 and lifestyle change + benzbromarone

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
artery stiffness parameter;

Secondary

MeasureTime frame
systolic blood pressure;diastolic blood pressure;CIMT;

Countries

China

Contacts

Public ContactWang Yong
wangyong1239117@sina.com+86 13801239117

Outcome results

None listed

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