Lower Silesia Culotte Bifurcation Registry (LSCBR).
Recruiting
Observational Study
Safety Issues
Efficacy, Self
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 400 (estimated)
- Sponsor
- Regional Cardiology Center, The Copper Health Centre (MCZ), · Other
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About This Trial
The study aimed to evaluate the outcomes of bifurcation PCI using two techniques (Culotte vs. DK-Culotte) using data from a retrospective analysis.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Presence of significant changes in the coronary bifurcation requiring the implantation of two coronary stents using the Culotte or DK Culotte technique.
Exclusion Criteria:
* Patients who underwent PCI with coronary stents prior to the index procedure for the bifurcation les…
Contacts