Coronary and Structural Interventions Ulm - Coronary Chronic Total Occlusions

Not Applicable

Completed

• Conditions: Stable Angina; Ischemic Heart Disease; Coronary Artery Disease
• Interventions: Device: stent or scaffold

• Registration Number: NCT02162082
• Lead Sponsor: University of Ulm

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.

Study Timeline

• Study Start: 2014-06
• Study First Submitted: 2014-06-07
• Study First Submitted QC: 2014-06-11
• Study First Posted: 2014-06-12
• Primary Completion: 2018-12-31
• Study Completion: 2018-12-31
• Status Verified: 2020-04
• Last Update Submitted: 2020-04-25
• Last Update Posted: 2020-04-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 198

Inclusion Criteria

• coronary artery disease
• chronic total occlusion

Exclusion Criteria

• no written informed consent

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
stent or scaffold	stent or scaffold	implantation of stents or scaffolds after recanalization of coronary chronic total occlusions

Primary Outcome Measures

Name	Time	Method
Major adverse cardiac events	1-5 years

Trial Locations

Locations (1)

University of Ulm; 🇩🇪 Ulm, Germany