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Clinical Trials/NCT01538186
NCT01538186
Completed
Not Applicable

Treatment Of Coronary Bifurcation Lesions: Stentcovering Of The Side Branch With And Without PCI Of The Side Branch: A Retrospective Analysis Of All Consecutive Patients

Krankenhaus Hetzelstift1 site in 1 country98 target enrollmentJanuary 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Bifurcation Lesions
Sponsor
Krankenhaus Hetzelstift
Enrollment
98
Locations
1
Primary Endpoint
Major adverse cardiac outcome
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

This retrospective observational study included patients (pts) with percutaneous coronary intervention (PCI) of a de novo coronary bifurcation lesion in one German center between January 2008 - August 2011. The investigators included all consecutive patients where the side branch was covered with a stent. Patients with ACS/cardiogenic shock were not excluded.

Two different methods were compared: group A represents patients with a simple strategy without any treatment of the side branch (SB). Group B consisted of patients where the SB was treated (PCI and/or stenting).

For the treatment of bifurcation lesions we used the concept of "provisional stenting", indications for the treatment of the SB were residual stenosis > 50 %, TIMI flow reduction < 2. Final-kissing PCI was intended in all patients of group B.

MACE during follow-up was evaluated in all patients.

Registry
clinicaltrials.gov
Start Date
January 2008
End Date
February 2012
Last Updated
14 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Krankenhaus Hetzelstift
Responsible Party
Principal Investigator
Principal Investigator

Hubertus von Korn, MD

Head of the Department

Krankenhaus Hetzelstift

Eligibility Criteria

Inclusion Criteria

  • All consecutive patients with a bifurcation lesion, where the side branch was covered with a stent placed inside the main branch.

Exclusion Criteria

  • Patients with an in-stent-restenosis, patients with a therapy using a drug coated balloon during the procedure (inside the main branch and/or the side branch) and patients where the side branch was not covered by the stent inside the main branch.

Outcomes

Primary Outcomes

Major adverse cardiac outcome

Time Frame: 12 months

Study Sites (1)

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