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Clinical Trials in Spain / NCT07206082
Active, not recruiting Observational

Coronary Laser in Undilatable or Uncrossable Lesions

NCT07206082 · tracked via the Priya Life Science Spain tracker
Phase
Observational
Started
2020-06-05
Last updated
2025-10-03

Condition(s) studied

Coronary Artery DiseaseCalcified Coronary Artery DiseaseIn Stent RestenosisChronic Total Occlusion (CTO)

Investigational drug(s) / intervention(s)

Laser atherectomy

Laser atherectomy: ELCA procedure will be performed using the Spectranetics CVX300 (Spectranetics, Colorado Spring, CO, USA) and the latest generation Philips Laser System Excimer (Philips, San Diego, CA, USA) System, which is based on pulsed xenon-chlorine laser catheters capable of delivering excimer energy (wavelength 308 nm, pulse length 185 ns) from 30 to 80 mJ/mm2 (fluencies) at pulse repetition rates from 25 to 80 Hz. The ELCA technique will be performed according to current recommendations (18). The laser probe size will be at the operator´s discretion among the available options (rapid exchange concentric 0.9 mm, 1.4 mm, 1.7mm or 2.0mm). The selection of fluence, and repetition rate will be left to the operator. A saline infusion technique will be recommended, although application of laser with blood or contrast will be recommended in resistant lesions. In the event of unsuccessful initial therapy, additional plaque modification techniques may be employed at the discretion of the operator and wi

Study summary

This will be an investigator-initiated, multicentre, single-arm, open-label, prospective observational study. Patients with indication for PCI and undilatable (non-compliant balloon dilatation \<80% at burst pressure) or uncrossable (not crossable with a "small-profile balloon" with adequate support, according to operator´s discretion) coronary lesions treated with ELCA will be included. Intravascular imaging will be highly recommendable and analysed in a central core-laboratory. Device success, angiographical success, procedural success, clinical success and related complications will be evaluated. Patients will be followed for 1 year after the procedure and clinical events will be recorded.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients aged over 18 years. * Patients with either stable coronary artery disease or acute coronary syndromes as the clinical presentation. * Patients with severe coronary lesions (\>70% by visual estimation) in native vessels or coronary bypass grafts. * "Uncrossable" coronary lesions (i.e., lesions that cannot be crossed with a 0.7:1 balloon after successful guidewire passage) or "Undilatable" lesions (i.e., those in which balloon dilation with a 1:1 non-compliant balloon at 18 atm results in less than 80% expansion relative to the distal reference vessel diameter; this group includes both de novo lesions and in-stent restenosis or underexpanded stents). Exclusion Criteria: * Patients with known allergies to aspirin (ASA), clopidogrel, prasugrel, or ticagrelor. * Patients unable to provide informed consent, either personally or through a legal representative. * Patients with clinical or hemodynamic instability defined as: sustained hypotension (systolic blood pressure ≤ 90 mmHg for ≥ 30 minutes or use of pharmacological and/or mechanical support to maintain an SBP ≥90 mmHg) or evidence of end-organ hypoperfusion including urine output of \<30 mL/h, cool extremities, altered mental status, and/or serum lactate \>2.0 mmol/L. * Patients with significant comorbidities and a life expectancy of less than one year.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hospital Universitario La Paz Madrid Madrid

More Hospital Universitario La Paz trials in Spain

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07206082 on ClinicalTrials.gov ↗ ← All trials in Spain