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Clinical research on spironolactone in the treatment of coronary heart disease with renal insufficiency based on heart and kidney remodeling

Clinical research on spironolactone in the treatment of coronary heart disease with renal insufficiency based on heart and kidney remodeling

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042510
Enrollment
Unknown
Registered
2021-01-22
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-05-03

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

Conditions

Coronary heart disease with renal insufficiency

Interventions

Spironolactone group:20mg spirolactone
Spironolactone combined with potassium-lowering drug group:20mg spironolactone+5mg Sodium Zirconium Cyclosilicate Powder

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Subjects over 18 years old; 2. Patients with clinical diagnosis of coronary heart disease: the results of coronary angiography showed that the diameter of coronary artery stenosis was more than 50%; 3. Patients with clinical diagnosis of chronic renal insufficiency: the history of renal injury was more than 3 months and glomerular filtration rate was less than 60 ml / min.1.73 m2; 4. Patients with blood potassium >= 3.5mmol/l <= 5.0mmol/l. 5. Patients who signed informed consent.

Exclusion criteria

Exclusion criteria: 1. In patients with liver dysfunction, transaminase was 3 times higher than the upper limit; 2. Patients with EGFR less than 30ml / min .1.73m2 and without renal replacement therapy (hemodialysis, peritoneal dialysis). 3. Patients who need metformin, aminoglycosides, amphotericin B, chemotherapy drugs, non steroidal anti-inflammatory drugs and other drugs for kidney damage during the trial; 4. Patients allergic to contrast medium; 5. Patients with severe cardiac insufficiency NYHA IV, myocardial infarction Killip III-IV, cardiogenic shock, malignant arrhythmia, etc. who need rescue before operation; 6. Patients with abnormal thyroid function; 7. Patients with acute cerebrovascular disease; 8. Patients with malignant tumor; 9. Patients with intraoperative complications; 10. Any situation in which the researcher believes that the patient's condition will hinder the clinical study.

Design outcomes

Primary

MeasureTime frame
aldosterone level;LVEF;LVEDV;type I and III collagen;

Secondary

MeasureTime frame
creatine;eGFR;BNP;

Countries

China

Contacts

Public ContactZhou Hao

The First Affiliated Hospital of Wenzhou Medical University

wyzh66@126.com+86 13968801939

Outcome results

None listed

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