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A Preliminary Study on the Efficacy and Safety of Lipibetai Combined with Atorvastatin in the Treatment of Chronic Kidney Disease with Dyslipidemia

A Preliminary Study on the Efficacy and Safety of Lipibetai Combined with Atorvastatin in the Treatment of Chronic Kidney Disease with Dyslipidemia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105643
Enrollment
Unknown
Registered
2025-07-08
Start date
2025-07-10
Completion date
Unknown
Last updated
2025-07-14

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

Conditions

Chronic kidney disease complicated with mixed dyslipidemia

Interventions

The group treated with Zhibite combined with atorvastatin:Based on the control group, Lipitai Capsules were added, 480mg each time, twice a day, orally. The treatment was maintained until the end.
Atorvastatin group:Atorvastatin Calcium Tablets, 10mg each time, once a day, oral administration, for maintenance treatment until the end.

Sponsors

Zhengzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Chronic kidney disease (CKD) combined with mixed dyslipidemia: triglyceride (TG) >= 2.3 mmol/L, low-density lipoprotein cholesterol (LDL-C) >= 3.4 mmol/L. 2. In the past 2 weeks, no other drugs affecting lipid metabolism have been taken. 3. The patient and his/her family members have been informed and signed the consent form.

Exclusion criteria

Exclusion criteria: 1. Those who are allergic to the drug under study; 2. Patients with active liver diseases or with persistent elevation of aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) for no apparent reason; 3. Pregnant women and lactating women; 4. Patients with acute infections in other parts such as peritonitis, urinary tract infection, pneumonia, etc.; 5. Patients with severe cardiovascular or cerebrovascular diseases; 6. Patients with malignant tumors, mental disorders, etc.

Design outcomes

Primary

MeasureTime frame
Determination of various lipid indicators: TG, TC, LDL-C, HDL-C, ApoA1, ApoB, Lp(a);

Countries

China

Contacts

Public Contacthemeng

Zhengzhou Central Hospital

zxyyhm@126.com+86 137 3389 8260

Outcome results

None listed

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