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NCT06577038Enrolling by invitation

Prospective Registry on Intravascular Lithotripsy

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

Source: ClinicalTrials.gov · Last updated 29 Aug 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
1000 (estimated)
First submitted
22 Jul 2024
Start date
1 May 2019
Primary completion date
1 Feb 2024
Lead sponsor
Leiden University Medical Center
NCT number
NCT06577038

What you commit to

  • Study type: Observational
  • Planned participants: 1000
  • From 1 May 2019 to the primary completion date, 1 Feb 2024
  • 8 sites in 3 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patient has any comorbidity or condition that, in the opinion of the Investigator, compromises the subject's ability to give written informed consent

Lab values

  • 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.

Who the study is looking for

  • Age \>18 years-old
  • Ability to provide written informed consent

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Cliniques universitaires Saint-Luc
Coordinator of this site? Confirm its status
BrusselsBelgiumUnknown status
Red Cross Hospital
Coordinator of this site? Confirm its status
AthensGreeceUnknown status
Amsterdam University Medical Center
Coordinator of this site? Confirm its status
AmsterdamNetherlandsUnknown status
Rijnstate Ziekenhuis
Coordinator of this site? Confirm its status
ArnhemNetherlandsUnknown status
Medisch Centrum Leeuwaarden
Coordinator of this site? Confirm its status
LeeuwardenNetherlandsUnknown status
Leiden University Medical Center
Coordinator of this site? Confirm its status
LeidenNetherlandsUnknown status
Radboud University Medical Center
Coordinator of this site? Confirm its status
NijmegenNetherlandsUnknown status
Jeroen Bosch Ziekenhuis
Coordinator of this site? Confirm its status
's-HertogenboschNetherlandsUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.