Skip to content

Effect of nicorandil on the prevention of contrast nephropathy in patients with coronary heart disease undergoing interventional therapy

Effect of nicorandil on the prevention of contrast nephropathy in patients with coronary heart disease undergoing interventional therapy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064264
Enrollment
Unknown
Registered
2022-10-01
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

contrast nephropathy

Interventions

Nicorandil routine dose group:On the basis of hydration, add oral nicorandil 5mg, TID from 1 day before operation to 4 days after operation
Nicorandil increased dose group:On the basis of hydration, add oral nicorandil 10mg, TID from 1 day before operation to 4 days after operation

Sponsors

Dongguan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The study is planned to enroll patients with renal insufficiency (defined as EGFR <= 60ml / min / 1.73m2) who will undergo coronary intervention from October 1, 2022 to September 30, 2024, aged 18-80 years, with contrast agent dosage greater than 60ml, and voluntarily sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with creatinine clearance rate <= 30ml / min / 1.73m2 and requiring hemodialysis; 2. Patients with contrast agent dosage < 60ml; 3. Patients allergic to nicorandil; 4. Known history of severe liver dysfunction; 5. Disease with systemic infection or its complications; 6. Previous malignant tumor history; 7. Glaucoma patients; 8. Pregnancy or lactation (pregnant women who may be pregnant should be examined for pregnancy); 9. Unable to comply with the trial protocol or follow-up requirements, or the researcher thinks that participating in the trial may cause the patient to face greater risks, or the researcher thinks that the enrollment of the subject may affect the special evaluation of the trial; 10. Other investigators considered that the patients were not suitable for enrollment.

Design outcomes

Primary

MeasureTime frame
Incidence of contrast nephropathy;

Countries

China

Contacts

Public ContactSuxia Guo

Dongguan People's Hospital

guo7771812@163.com+86 13665103927

Outcome results

None listed

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