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 @ 4:25 PM
Ignite Modification Date:
2025-12-24 @ 4:25 PM
NCT ID:
NCT01771666
Eligibility Criteria:
Inclusion Criteria:
* Ability to understand and the willingness to sign a written informed consent document.
* Signed written informed consent.
* Women undergoing sentinel lymph node biopsy.
* Women with breast cancer with known or suspected lymph node involvement.
* Women undergoing sentinel node identification and completion axillary lymph node dissection.
* Women of 18 years of age or older.
* Eastern Cooperative Oncology Group (ECOG) or Karnofsky Performance Status 0,1,2.
* Complete Blood Count (CBC) and basic Metabolic Panel within 6 months
Exclusion Criteria:
* History of liver or kidney failure will not be eligible.
* Allergies to iodine containing products will not be eligible.
* Women who are pregnant will not be eligible.
* Psychiatric or addictive disorders or other conditions that, in the opinion of the investigator, would preclude the patient from meeting the study requirements.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
90 Years
Study:
NCT01771666
Study Brief:
Protocol Section:
NCT01771666