Coronary and Structural Interventions Ulm - Coronary Chronic Total Occlusions

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02162082

Acronym

CSI-Ulm-CTO

Enrollment

198

Registered

2014-06-12

Start date

2014-06-30

Completion date

2018-12-31

Last updated

2020-04-28

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

Conditions

Coronary Artery Disease, Ischemic Heart Disease, Stable Angina

Brief summary

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

Detailed description

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

Interventions

DEVICEstent or scaffold

implantation of a CE certified drug-eluting stent, bare-metal stent or scaffold

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* coronary artery disease * chronic total occlusion

Exclusion criteria

* no written informed consent

Design outcomes

Primary

Measure	Time frame
Major adverse cardiac events	1-5 years

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026