Eligibility Module

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: 2025-12-24 @ 3:30 PM
Ignite Modification Date: 2025-12-24 @ 3:30 PM
NCT ID: NCT01367392
Eligibility Criteria: Inclusion Criteria: * Male or non-pregnant female subjects, between the ages of 18 and 80 at the time of enrollment. * Subjects scheduled for clinically indicated CT guided percutaneous needle placements in the liver who meet the desired target population described above. * Written informed consent to participate in the study. * Ability to comply with the requirements of the study procedures. * Verified home address and phone number to facilitate study follow-up. Exclusion Criteria: * Significant coagulopathy that cannot be adequately corrected. * Subjects who participated in an active stage of any drug, intervention or treatment trial within 30 days of enrollment. * Subjects with preexisting conditions, which, in the opinion of the investigator, interfere with the conduct of the study. * Subjects who are uncooperative or cannot follow instructions. * Mental state that may preclude completion of the study procedure. * Pregnant or nursing female subjects.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 80 Years
Study: NCT01367392
Study Brief:
Protocol Section: NCT01367392