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Registry Following Patients with Calcified Heart Artery Blockages Treated with Lithotripsy Balloon

Records how a lithotripsy device is used to open hardened coronary artery blockages in adults.

Plain-language title generated from the registry record
Registry title: Prospective Registry on Intravascular Lithotripsy

Key facts

Where
Athens, GreeceSee the site

Where in Greece

  • Red Cross HospitalAthens, GreeceNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Leiden University Medical Center
Trial code
NCT06577038
Record updated
29 August 2024
Original description
multicenter, international, all-comers registry aims to provide insights in the current application of IVL technology in patients with calcified coronary lesions undergoing PCI using IVL technology.Read full original descriptionShow less

Prospective, International, Multicenter, All-comers Registry for the Study of Intravascular Lithotripsy in Coronary Interventions

multicenter, international, all-comers registry aims to provide insights in the current application of IVL technology in patients with calcified coronary lesions undergoing PCI using IVL technology.

Inclusion: Age >18 years-old; Ability to provide written informed consent.

Exclusion: Patient has any comorbidity or condition that, in the opinion of the Investigator, compromises the subject's ability to give written informed consent; Patient belongs to a vulnerable population Subject is a member of a vulnerable population , including individuals with mental disability, persons in nursing homes, children, impoverished persons, persons in emergency situations, homeless persons, nomads, refugees, and those incapable of giving informed consent. Vulnerable populations also may include members of a group with a hierarchical structure such as university students, subordinate hospital and laboratory personnel, employees of the Sponsor, members of the armed forces, and persons kept in detention.

ClinicalTrials.gov NCT06577038