Clinical Trials Directory

Trials / Unknown

UnknownNCT02787317

Bivalirudin in Stable Ischemic Heart Disease Patients Undergoing PCI

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
1,770 (estimated)
Sponsor
Chinese PLA General Hospital · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Prolonging infusions may decrease myocardial damage associated with bivalirudin use during primary PCI. The investigators hypothesized that continuing the bivalirudin infusion commenced during the procedure at the PCI recommended dose for 4 hours would prevent myocardial damage.

Detailed description

Bivalirudin is widely used as an anticoagulant during percutaneous coronary intervention (PCI) for coronary heart disease. Prolonging infusions may decrease myocardial damage associated with bivalirudin use during primary PCI . However, whether prolonging infusions of bivalirudin could prevent ischemic complications is unknown. The investigators examined the effects of prolonged drug infusion after elective PCI. The investigators hypothesized that continuing the bivalirudin infusion commenced during the procedure at the PCI recommended dose for 4 hours would prevent myocardial damage.

Conditions

Interventions

TypeNameDescription
DRUGbivalirudinBivalirudin is an alternative to heparin in patients undergoing percutaneous coronary intervention.
DRUGHeparinHeparin is used in patients undergoing percutaneous coronary intervention.

Timeline

Start date
2016-05-01
Primary completion
2017-10-01
Completion
2018-11-01
First posted
2016-06-01
Last updated
2016-06-01

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT02787317. Inclusion in this directory is not an endorsement.