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Clinical Study of Bivalirudin for Percutaneous Coronary Intervention (PCI)

Safety and Efficacy of Bivalirudin in Patients With Diabetes Mellitus Undergoing Percutaneous Coronary Intervention (PCI)

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03567408
Enrollment
200
Registered
2018-06-25
Start date
2018-09-15
Completion date
2020-08-12
Last updated
2018-08-20

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

Conditions

Coronary Heart Disease

Brief summary

Bivalirudin is widely used as an anticoagulant to reduce the risk of bleeding in PCI perioperative period. Additionally, 15.7%-32.7% patients have diabetes mellitus who undergo percutaneous coronary interventions (PCI), so bivalirudin was used to anticoagulate in these patients to evaluate its safety and efficacy.

Detailed description

Bivalirudin is a specific reversible thrombin direct inhibitor and the function of thrombin activity site can be recovered through hydrolyzing bivalirudin by thrombin. Therefore, bivalirudin is widely used as an anticoagulant during percutaneous coronary intervention (PCI) for coronary heart disease, and 15.7%-32.7% patients have diabetes mellitus who undergo percutaneous coronary interventions (PCI). At the same time, elderly patients have higher risk of bleeding whose age over 65, so bivalirudin can reduce the risk of bleeding and the incidence of net adverse clinical events for the elderly patients whose age over 65 with diabetes mellitus in PCI perioperative period.

Interventions

PROCEDURESelective PCI

Selective PCI for treatment of elderly patients (age≥65) presenting with diabetes mellitus.

DRUGBivalirudin

Before, during and after surgery, bivalirudin was used according to the dosage regimen to assess it's impact on elderly patients with diabetes mellitus undergoing selective PCI.

Sponsors

Qian Gong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. ≥ 65 years, with diabetes mellitus. 2. Patients who undergo selective PCI therapy. 3. Patients who agree to participate in this clinical trial and sign informed consent prior to surgery.

Exclusion criteria

1. Patients with acute coronary syndrome undergoing primary PCI. 2. Combined with other diseases, the life expectancy of patients don't exceed 1 year. 3. Patients with active bleeding. 4. Bleeding in the gastrointestinal or urogenital tract in the past 6 weeks. 5. Combined with high risk of postoperative hemorrhage, such as active gastric ulcer, active ulcerative colitis, etc. 6. Patients who have undergone major surgery in the last 1 month. 7. A history of intracranial bleeding or structural abnormalities, such as cerebral aneurysms. 8. Patients with cardiogenic shock, or suspected myocarditis, infective endocarditis. 9. Patients who received regular heparin therapy within 6 hours or low molecular weight heparin therapy within 8 hours, or other factors that the researchers believe may influence the outcome of the trial. 10. Patients with severe uncontrolled hypertension. 11. Patients with active hepatitis, HIV and other infectious diseases. 12. Patients with contraindications of bivalirudin and heparin. 13. Other researchers considered the patients are unfit to participate in this study.

Design outcomes

Primary

MeasureTime frameDescription
activated clotting time(ACT)5min after using drugThe ACT test can be used to monitor anticoagulation effects, such as high-dose heparin before, during, and shortly after procedures that require intense anticoagulant administration, such as cardiac bypass, cardiac angioplasty, thrombolysis, extra-corporeal membrane oxygenation (ECMO) and continuous dialysis

Secondary

MeasureTime frameDescription
30-day major adverse cardiac events30 days30-day major adverse cardiac events including recidivation of angina pectoris, in-stent restenosis, severe arrhythmia, cardiac failure, sudden cardiac death.
30-day bleeding events30 daysAccording to the bleeding academic research consortium (BARC) bleeding classification.

Contacts

Primary ContactQian Gong, Master
1500113940@qq.com15583407654

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026