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Study for the efficacy and safety of Xue-Zhi-Kang combined with ezetimibe in the treatment of non-dialysis chronic renal disease patients

Study for the efficacy and safety of Xue-Zhi-Kang combined with ezetimibe in the treatment of non-dialysis chronic renal disease patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016885
Enrollment
Unknown
Registered
2018-06-30
Start date
2018-07-09
Completion date
Unknown
Last updated
2018-07-02

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

Conditions

non-dialysis chronic kidney diseases

Interventions

Group 1:Xuezhikang 0.6g bid
Group 2:Xuezhikang 0.6g bid and Ezetimibe 10mg qd
Group 3:Atorvastatin 20mg qn

Sponsors

Second Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Any of the following items shall be satisfied for more than 3 months: (1) abnormal blood: BUN and Cr.(2) urine: hematuria, proteinuria (3) renal imaging abnormalities (4) renal pathological changes (5) glomerular filtration rate 2.6 mmol/L or severe CKD and CKD combined with hypertension or diabetes mellitus had ldl-c > 1.8 mmol/L.

Exclusion criteria

Exclusion criteria: 1. Secondary causes of myopathy (including myositis and rhabdomyolysis) or elevated liver enzymes, such as physical exercise, drug action, liver disease, etc.; 2. Patients with persistent dialysis or eGFR < 30ml/min.1.73m2; 3. Patients who are contraindicated or allergic to the use of xuezhikang; 4. Pregnant and lactating patients.

Design outcomes

Primary

MeasureTime frame
LDL-C;TC;TG;HDL-C;CCr;BUN;CK;CKMB;ALT;AST;MACEs;

Secondary

MeasureTime frame
hsCRP;TGF-ß;

Countries

China

Contacts

Public ContactQiang She

Second Affiliated Hospital of Chongqing Medical University

qshe98@hotmail.com+86 13508393602

Outcome results

None listed

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