Coronary and Structural Interventions Ulm - Coronary Chronic Total Occlusions (CSI-Ulm-CTO)

University of Ulm

Status: Completed

Conditions: Ischemic Heart Disease; Coronary Artery Disease; Stable Angina

Treatments: Device: stent or scaffold

Study type: Interventional

Funder types: Other

Identifiers

NCT02162082

CSI Ulm - CTO 1.0

Details and patient eligibility

About

To evaluate the long-term results after recanalization of coronary chronic total occlusions.

Full description

Patients with successful recanalization of coronary chronic total occlusions are followed during a period of 5 years to demonstrate safety and efficacy.

Enrollment: 198 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• coronary artery disease
• chronic total occlusion

Exclusion criteria

• no written informed consent

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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198 participants in 1 patient group

stent or scaffold

Experimental group

Description:

implantation of stents or scaffolds after recanalization of coronary chronic total occlusions

Treatment:

Device: stent or scaffold