CELTIC Bifurcation Study

NCT02232815 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 170

Last updated 2016-09-07

No results posted yet for this study

Summary

This study will examine outcomes for patients treated by planned culotte stenting and compare outcomes with 2 different stent platforms, the next generation Synergy II and the Xience Xpedition DES platforms.

Conditions

  • Coronary Bifurcations

Sponsors & Collaborators

  • Ceric Sàrl

    collaborator INDUSTRY
  • European Cardiovascular Research Center

    lead NETWORK

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-12-31
Primary Completion
2016-12-31
Completion
2018-12-31

Countries

  • Ireland
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02232815 on ClinicalTrials.gov