drugset / Trial / NCT06730945

Effect of Oral Isosorbide Mononitrate Plus Amlodipine Antispasm Therapy on Outcomes of Radial Artery Grafts After CABG

NCT06730945

Phase 4 Withdrawn Ruijin Hospital
RandomizedParallel-groupSingle-blindTreatment

Summary

The goal of this clinical trial is to to evaluate the effect of oral isosorbide mononitrate plus amlodipine antispasm therapy on outcomes of radial artery grafts in patients underwent primary isolated CABG. The main question it aims to answer is: Whether the oral isosorbide mononitrate plus amlodipine antispasm therapy could reduce the failure outcome of radial artery grafts after CABG . Researchers will compare isosorbide mononitrate plus amlodipine to none to see if isosorbide mononitrate plus amlodipine works. Participants will 1. Take oral isosorbide mononitrate (20-40mg daily) plus amlodipine (2.5-5mg daily) therapy for 24 weeks after CABG. 2. Clinical follow-up at Week 1, 4, 12, and 24 after CABG. 3. Protocol-driven CCTA at Week 24 after CABG.

Timeline

Start
2025-06
Primary completion
2028-12
Completion
2030-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Amlodipine Other / unclassified 2.5 mg Oral
Subject Amlodipine Other / unclassified 5 mg Oral
Subject Isosorbide Mononitrate Other / unclassified 20 mg Oral
Subject Isosorbide Mononitrate Other / unclassified 40 mg Oral

Indications

No indication recorded.