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The effect of breviscapine on the viable myocardium and left ventricular remodeling after revascularization of coronary chronic total occlusion

The effect of breviscapine on the viable myocardium and left ventricular remodeling after revascularization of coronary chronic total occlusion

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPC-16010161
Enrollment
Unknown
Registered
2016-12-15
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Cardiovascular Disease

Interventions

breviscapine:breviscapine
Control:Placebo

Sponsors

SIR RUN RUN SHAW Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years; 2. Coronary CT or Coronary angiograme verified at least one main vessel totally occlusion in left/right coronary artery.

Exclusion criteria

Exclusion criteria: 1. AMI in 1 week; 2. The target lesion was done PCI or CABG in the last 6 months; 3. Will have surgical operation(except CABG) in the future 6 months; 4. Cerebral infaction in the last 6 months; 5. Can not tolerate dual anti-platelet or statin therapy, or allergy to breviscapine; 6. Using breviscapine at this time; 7. Combine with server hepatic or respiratory dysfunction; 8. Heart Failure (NYHA IV), or EF3mg/dl or eGFR <40 ml/min/1.73 m2; 10. Combined with dilated cardiomyopathy, hypertrophic cardiomyopathy or server valvular heart disease; 11. Will or just using glucocorticoid; 12. Combined with malignant tumor; 13. Predicted survival <12 months; 14. Pregnancy test positive; 15. Participate in another clinical trial, or will participate in the future 12 months.

Design outcomes

Primary

MeasureTime frame
The comparation of viable myocardium at 12 months with baseline;

Secondary

MeasureTime frame
MACE;left ventricular remodeling;The comparation of viable myocardium at 1 months with baseline;The comparation of microcirculatory perfusion at 1/12 months with baseline;VEGF and bFGF concentration at peripheral blood;

Countries

China

Contacts

Public ContactWENBIN ZHANG

SIR RUN RUN SHAW Hospital

wzhang_crf@126.com+86 13777572567

Outcome results

None listed

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