Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:15 PM
Ignite Modification Date:
2026-03-26 @ 3:15 PM
NCT ID:
NCT07417150
Eligibility Criteria:
Inclusion Criteria:
* Male or female aged 18 years or older
* Patient with a coronary lesion.
* Angiographically calcified culprit lesion (Mintz classification) 1 Moderate: lesion with radiopaqueness noted only during the cardiac cycle before contrast injection Severe: lesion with radiopaqueness seen without cardiac motion before contrast injection, visible on both sides of the arterial lumen
* Ability to traverse the culprit lesion with an IVUS catheter
* Having been informed by an investigator about the research topic and having given their free, explicit, and informed consent.
* Affiliation with a social security scheme (beneficiary or dependent)
Exclusion Criteria:
* Acute coronary syndrome of the ST-segment elevation myocardial infarction type
* Progressive cardiogenic shock
* Culprit lesion impassable with an IV catheter
* Pregnant, parturient, or breastfeeding women and other vulnerable categories: legally incapacitated adults, adults unable to express their consent and not subject to a protective measure, persons deprived of their liberty
* BMI \> 35 kg/m²
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07417150
Study Brief:
Protocol Section:
NCT07417150