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 @ 12:10 AM
Ignite Modification Date:
2025-12-25 @ 12:10 AM
NCT ID:
NCT01329458
Eligibility Criteria:
Inclusion Criteria:
* patients diagnosed with de novo FLL at standard ultrasound
* age \> 18 years, male and female gender
* informed consent for the contrast enhanced study
Exclusion Criteria:
* patients with contraindication for contrast enhanced study: subjects with acute cardiac infarction, with class III/IV cardiac insufficiency, with rhythm disorders and pregnant women
* Patients diagnosed with simple cysts at standard ultrasound (biliary of hydatid)
* Patients with known FLL, for example after percutaneous treatment, in which the contrast study is used for the follow up of the patient.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01329458
Study Brief:
Protocol Section:
NCT01329458