drugset / Trial / NCT01465503

Novel Approaches in Preventing and Limiting Events III Trial (NAPLES III): Bivalirudin in High-risk Bleeding Patients

NCT01465503

Phase 3 Completed 837 enrolled Clinica Mediterranea
RandomizedParallel-groupDouble-blindPrevention

Summary

Bleeding occurring during percutaneous coronary interventions (PCI has now emerged as one of the most common complication of PCI and adversely affect in-hospital, short- and long-term outcome.As bivalirudin proved its effectiveness in decreasing haemorrhagic events during PCI, its administration may be advocated in subjects deemed at high risk of bleeding.Objective of the present trial is to compare the safety and effectiveness of procedural use of bivalirudin in comparison to unfractionated heparin (UFH) in patients undergoing PCI deemed at high risk of procedural bleeding.

Timeline

Start
2008-01
Primary completion
2012-12
Completion
2013-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bivalirudin Peptide 1 mg/kg
Comparator Bivalirudin Peptide 1.75 mg/kg
Comparator Heparin Other / unclassified 70 iu/kg

Indications