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:
2025-12-25 @ 2:32 AM
Ignite Modification Date:
2025-12-25 @ 2:32 AM
NCT ID:
NCT02493634
Eligibility Criteria:
Inclusion Criteria:
* patients with clinical indication for cardiac magnetic resonance and conventional diagnostic catheterisation
* patients with body weight of \> 40 kg in which the introduction of an introducer of \> 5 French is possible.
* subject provided written informed consent using the approved consent form or in case of a minor the subject provided written assent and its legal guardian provided written informed consent.
Exclusion Criteria:
* major surgery in the last 42 days
* history of irreversible bleeding disorder
* contraindication to cardiac magnetic resonance
* Contraindications to guidewire procedures, such as evidence of active infection
* women of child-bearing potential who cannot provide a negative pregnancy test
* chronic total occlusion.
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT02493634
Study Brief:
Protocol Section:
NCT02493634