Ignite Creation Date:
2024-05-06 @ 8:10 PM
Last Modification Date:
2024-10-26 @ 3:22 PM
Study NCT ID:
NCT06284057
Status:
RECRUITING
Last Update Posted:
2024-03-06
First Post:
2024-02-21
Brief Title:
Lower Silesia Culotte Bifurcation Registry LSCBR
Sponsor:
Regional Cardiology Center The Copper Health Centre MCZ
Organization:
Regional Cardiology Center The Copper Health Centre MCZ
Study Overview
Official Title:
Double Kissing DK vs Culotte Culotte Lower Silesia Culotte Bifurcation Registry LSCBR
Status:
RECRUITING
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
LSCBR
Brief Summary:
The study aimed to evaluate the outcomes of bifurcation PCI using two techniques Culotte vs DK-Culotte using data from a retrospective analysis
Detailed Description:
The study contains a retrospective analysis of subjects who have undergone PCI in two high-volume cooperative Cardiac Departments in the Lower Silesia Region Poland between April 2012 and January 2024 Data regarding all performed PCI from these periods were prescreened in terms of bifurcation lesion with subsequent implantation of two stents using the Culotte technique or the DK-Culotte technique The indication for percutaneous coronary intervention PCI was based either on a judgment made by the Heart Team or on a particular clinical indication ongoing ischemia lack of will for the alternative treatment options presence of significant angiographic CAD suitable for PCI due to ESCESH recommendation The decision to perform the two-stent technique PCI was left to the operators dissertation based on clinical and angiographical features All patients were thoroughly informed about all therapeutic options and PCI-related risks before providing written informed consent for the procedure There were no clinical or vessel-related exclusion criteria lesion anatomy length tortuosity severity However patients who had undergone PCI with coronary stents prior to the index procedure with respect to the bifurcation lesion studied were excluded from the study
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None