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.
Study Type
OBSERVATIONAL
Enrollment
170
St Vincent's Hospital Dublin
Dublin, Ireland
RECRUITINGBelfast Health & Social Care Trust
Belfast, United Kingdom
RECRUITINGBristol Royal Infirmary
Bristol, United Kingdom
Composite measure of Adverse events
Composite of: * Death * Myocardial Infarction * CVA * Target Vessel Failure (Composite of Target Vessel Revascularization and Target Vessel Inadequacy) * Definite or Probable stent thrombosis (ARC criteria \[14\]) * Binary angiographic restenosis
Time frame: 9 months
Technical success (deployment of stents in both branches with <20% residual stenosis and kissing balloon inflation at end of procedure)
Time frame: Day 0, during procedure
Total procedure time
Time frame: Day 0, during procedure
Total radiation dose
Time frame: Day 0, during procedure
Need to use secondary equipment or manoeuvres to complete the case
extra support guidewires, anchor balloons or mother \& daughter catheter
Time frame: Day 0, during procedure
Evidence of longitudinal stent compression at index implantation
Time frame: Day 0, during procedure
Evidence of stent fracture at angiographic follow-up
Time frame: Day 0, during procedure
Composite measure of Adverse events
Composite of: * Death * Myocardial Infarction * CVA * Target Vessel Failure (Composite of Target Vessel Revascularization and Target Vessel Inadequacy) * Definite or Probable stent thrombosis (ARC criteria \[14\])
Time frame: 24 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Edinburgh Royal Infirmary
Edinburgh, United Kingdom
RECRUITINGGolden Jubilee
Glasgow, United Kingdom
RECRUITINGKings College
London, United Kingdom
RECRUITING