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Clinical Trials/NCT02162082
NCT02162082CompletedNot Applicable

Coronary and Structural Interventions Ulm - Coronary Chronic Total Occlusions

University of Ulm2 sites in 1 country198 target enrollmentStarted: June 1, 2014Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
198
Locations
2
Primary Endpoint
Major adverse cardiac events
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

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 Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •coronary artery disease
  • •chronic total occlusion

Exclusion Criteria

  • •no written informed consent

Outcomes

Primary Outcomes

Major adverse cardiac events

Time Frame: 1-5 years

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University of Ulm
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jochen Wohrle

Prof. Dr. Jochen Wöhrle

University of Ulm

Study Sites (2)

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