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 @ 5:58 PM
Ignite Modification Date:
2025-12-24 @ 5:58 PM
NCT ID:
NCT06304168
Eligibility Criteria:
Inclusion Criteria:
* Aim 1 Tissue
* Cases:
* Patient has a biopsy confirmed diagnosis of target histology
* Tissue samples from synchronous or metachronous primary cancers may be used as long as they are clearly of a different target organ.
* Tumors from patients with an underlying genetic disorder pre-disposing to cancer may be included as long as they are stratified from those without
* Controls:
* Patient does not have the diagnosis of target histology
* Aim 2 Blood
* Cases:
* Patient has a biopsy confirmed diagnosis of target histology or radiographic criteria that are unequivocal for diagnosis (example, meets radiographic criteria for hepatocellular carcinoma)
* Controls:
* Patient does not have a diagnosis of the target histology
* Aim 3 Urine
* Cases:
* Patient has a biopsy confirmed diagnosis of target histology or radiographic criteria that are unequivocal for diagnosis (example, meets radiographic criteria for hepatocellular carcinoma)
* Controls:
* Patient does not have a diagnosis of the target histology
Exclusion Criteria:
* Aim 1 Tissue
* Cases and Controls:
* Patient has had any transplants prior to tissue collection
* Patient has received chemotherapy class drugs within 5 years prior to tissue collection
* Cases:
* Patient has had radiation to the current target lesion prior to tissue collection
* Patient has multi-centric/multi-focal breast cancer with differing genetic profiles (ER/HER2/PR status differ; if multiple masses are present and not all are tested then exclude patient)
* Patient has bilateral breast cancer/Ductal carcinoma in situ (DCIS)
* Aim 2 Blood
* Cases and Controls:
* Patient has known cancer outside of the target cancer 5 years prior to blood collection (not including basal cell or squamous cell skin cancers)
* Patient has received chemotherapy class drugs in the 5 years prior to blood collection
* Patient has had any prior radiation therapy to the target lesion prior to blood collection
* Patient has had a biopsy to the target organ and/or lesion within 3 days before blood collection
* Cases:
* Patient has had an intervention to completely remove current target pathology
* The current target pathology is a recurrence
* Patient has multi-centric/multi-focal breast cancer with differing genetic profiles (ER/HER2/PR status differ; if multiple masses are present and not all are tested then exclude patient)
* Patient has bilateral breast cancer/DCIS
* Aim 3 Urine
* Patient has known cancer outside of the target cancer 5 years prior to urine collection (not including basal cell or squamous cell skin cancers)
* Patient has received chemotherapy class drugs in the 5 years prior to urine collection
* Patient has had any prior radiation therapy to the target lesion prior to urine collection
* Patient has had a biopsy to the target organ and/or lesion within 3 days before urine collection
* The current target pathology is a recurrence
* Patient has chronic indwelling urinary catheter
* Patient has had a urinary tract infection within the 14 days prior to sample collection
* If patient does not have a primary bladder, ureter or urethral cancer, patient has a history of bladder ureter, or urethral cancer
* Cases:
* Patient has had an intervention to completely remove current target pathology
* The current target pathology is a recurrence
* Patient has multi-centric/multi-focal breast cancer with differing genetic profiles \[estrogen receptor (ER)/human epidermal growth factor receptor 2 (HER2)/progesterone receptor (PR)\] status differ; if multiple masses are present and not all are tested then exclude patient)
* Patient has bilateral breast cancer/DCIS
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06304168
Study Brief:
Protocol Section:
NCT06304168