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Coronary Bifurcation Lesions clinical trials

View clinical trials related to Coronary Bifurcation Lesions.

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NCT ID: NCT03172845 Completed - Clinical trials for Coronary Bifurcation Lesions

Optical Coherence Tomography (OCT) Findings and Coronary Bifurcation Lesions

Start date: June 27, 2017
Phase: N/A
Study type: Interventional

To determine the clinical prevalence of vulnerable plaque using OCT in patients with coronary bifurcation lesion.

NCT ID: NCT03027830 Completed - Clinical trials for Coronary Bifurcation Lesions

iFR Pressure Wires in Assessment of the Provisional Side-branch Intervention Strategy for Bifurcation Lesions

Start date: March 2014
Phase: N/A
Study type: Interventional

Even in the era of drug-eluting stents, bifurcation lesions remain one of the most challenging lesion subsets in coronary intervention practice. This study was performed to evaluate the functional outcomes of pressure wires (IFR)-guided jailed side-branch intervention strategy.

NCT ID: NCT01538186 Completed - Clinical trials for Coronary Bifurcation Lesions

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

Start date: January 2008
Phase: N/A
Study type: Observational

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.