Drug Eluting Pantera Lux Catheter Registry

Biotronik

Status: Completed

Conditions: Coronary Artery Disease

Study type: Observational

Funder types: Industry

Identifiers

NCT01081366

C0905 DELUX

Details and patient eligibility

About

All comers registry - Evaluation of the safety and efficacy of the Pantera Lux Paclitaxel releasing balloon for coronary arteries in daily clinical practice.

Full description

All patients are treated with the Pantera Lux Paclitaxel releasing balloon.

Clinical follow ups at 1, 6 and 12 months after coronary intervention.

Enrollment: 1,064 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria:

• Signed Patient Informed Consent / Data Release Form
• Patient eligible for percutaneous coronary intervention (PCI)
• Patient is older than 18 years of age

Exclusion Criteria

• Patient has a known allergy against appropriate anticoagulation / antiplatelet therapy
• Patients with known allergy against paclitaxel or BTHC
• Patients with a target lesion that was previously treated by brachytherapy
• Pregnant woman or lactating woman