Coronary Laser Atherectomy Registry From an International Taskforce
Recruiting now
Conditions studied: Stable Coronary Artery Disease, Acute Coronary Syndromes
In brief
This study is a prospective, investigator-initiated, multi-center, single arm, observational registry of performance of Excimer Laser Coronary Atherectomy (ELCA) in standard use cases of percutaneous coronary intervention (PCI).
Key facts
- Study ID
- NCT07348341
- Run by
- Ceric Sàrl
- People needed
- 500
- Starts
- 2026-07-20
- Expected to finish
- 2029-07-30
- Last updated by the study team
- 2026-07-23
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects will be included if all the following criteria are met:
- Age 18 years or over
- Patient willing to be included in the registry
- Patients with stable coronary artery disease or acute coronary syndromes with de-novo or intra-stent restenosis (ISR) coronary lesions suitable to be treated with ELCA
- Non-Crossable with ICI catheter or:
- Crossable with ICI catheter with significant calcium score suggesting need for calcium modification based on IVUS or OCT criteria and/or
- Non-Dilatable with 1:1 NC balloon
- Mandated use of ICI:
- Attempted before use of ELCA or
- Following ELCA and any other calcium modification strategy utilized (to evaluate whether the additional modification demonstrates significant additional modification of the calcium on ICI)
- Final after DES implantation or prior to use of DCB
- Declared PCI strategy (planned use of ELCA, need for IVL/specialty balloons/alternative atherectomy and stent strategy) prior to PCI procedure
You may not qualify if…
- Pregnant or breast feeding
- Unable to give informed consent
- PCI performed without IVCI attempt
- No ELCA use
- Allergy to clopidogrel, prasugrel or ticagrelor or non-compliance
- Post- cardiac arrest or haemodynamic instability
- Participation in another trial.
Where it is running
- La Paz Universtity Hospital — Madrid, Spain (enrolling)
Full record on ClinicalTrials.gov
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