Synergy Stent
DevicePatients with narrowed coronary artery disease qualifying for PCI were treated with Synergy stent implantation.
Other names: Synergy Coronary Stent
NCT Number: NCT02881216
This study sought to compare procedural performance of a new coronary stent generation, that is already available in Germany, with hitherto established current drug-eluting stents.
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Notify Me18 year–99 year
All sexes
Interventional
Not applicable
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients with narrowed coronary artery disease qualifying for PCI were treated with Synergy stent implantation.
Other names: Synergy Coronary Stent
Patients with narrowed coronary artery disease qualifying for PCI were treated with DES implantation (Xience Prime, Resolute Integrity, Promus Element Plus)
Other names: DES including Xience Prime, Resolute Integrity, Promus Element Plus.
Time frame: One week post-procedure
In-hospital major cardiac adverse events were collected up to one week after procedure throughout the in-patients stay
University Hospital Heidelberg
Other
Procedural Advantages of a Novel Drug-Eluting Coronary Stent With Ultra-Thin Struts and Bioabsorbable Abluminal Polymer Coating in an All-Comers Registry
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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