Gender and Age
Item
male aged 21 years or older
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Informed consent and compliance with protocol requirements
Item
ability to provide signed informed consent and willingness to comply with protocol requirements.
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
past biopsy indicating the presence of adenocarcinoma of the prostate gland
Item
past biopsy indicating the presence of adenocarcinoma of the prostate gland
boolean
C0007112 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C0005558 (UMLS CUI [1,3])
participant is deemed to have tissue suspicious of prostate cancer involvement that is amenable to biopsy/resection
Item
participant is deemed to have tissue suspicious of prostate cancer involvement that is amenable to biopsy/resection.
boolean
C0040300 (UMLS CUI [1,1])
C0242114 (UMLS CUI [1,2])
C0600139 (UMLS CUI [1,3])
C3900053 (UMLS CUI [1,4])
C0005558 (UMLS CUI [1,5])
C0040300 (UMLS CUI [2,1])
C0242114 (UMLS CUI [2,2])
C0600139 (UMLS CUI [2,3])
C3900053 (UMLS CUI [2,4])
C0728940 (UMLS CUI [2,5])
diagnostic CT or MRI prior to surgery
Item
have had, or will undergo diagnostic CT or MRI imaging prior to surgery
boolean
C1301732 (UMLS CUI [1,1])
C0011923 (UMLS CUI [1,2])
C0040405 (UMLS CUI [1,3])
C0332152 (UMLS CUI [1,4])
C0543467 (UMLS CUI [1,5])
C1301732 (UMLS CUI [2,1])
C0011923 (UMLS CUI [2,2])
C0917711 (UMLS CUI [2,3])
C0332152 (UMLS CUI [2,4])
C0543467 (UMLS CUI [2,5])
C0205156 (UMLS CUI [3,1])
C0011923 (UMLS CUI [3,2])
C0040405 (UMLS CUI [3,3])
C0332152 (UMLS CUI [3,4])
C0543467 (UMLS CUI [3,5])
C0205156 (UMLS CUI [4,1])
C0011923 (UMLS CUI [4,2])
C0917711 (UMLS CUI [4,3])
C0332152 (UMLS CUI [4,4])
C0543467 (UMLS CUI [4,5])
Agreeing to acceptable birth control throughout study and using condoms after study drug administration
Item
participants must agree to use an acceptable form of birth control throughout the study period. participants must use condoms for a period of seven days after study drug administration, if engaged in sexual activity.
boolean
C0700589 (UMLS CUI [1,1])
C2347804 (UMLS CUI [1,2])
C3641827 (UMLS CUI [1,3])
C0679782 (UMLS CUI [2,1])
C0580203 (UMLS CUI [2,2])
C3469597 (UMLS CUI [2,3])
C0304229 (UMLS CUI [2,4])
Participating would significantly delay the scheduled standard of care therapy
Item
participants for whom participating would significantly delay the scheduled standard of care therapy
boolean
C2348568 (UMLS CUI [1,1])
C0678227 (UMLS CUI [1,2])
C0205421 (UMLS CUI [1,3])
C2936643 (UMLS CUI [1,4])
Recent administration of radioisotope
Item
participants administered a radioisotope within 5 physical half lives prior to study enrollment
boolean
C0332185 (UMLS CUI [1,1])
C1533734 (UMLS CUI [1,2])
C0034595 (UMLS CUI [1,3])
C0259911 (UMLS CUI [2])
Medical condition or other circumstances impeding obtaining reliable data, achieving study objectives or completing study
Item
participants with any medical condition or other circumstances that, in the opinion of the investigator, would significantly decrease obtaining reliable data, achieving study objectives or completing the study
boolean
C3843040 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C3858758 (UMLS CUI [1,3])
C0681873 (UMLS CUI [1,4])
C3843040 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C2985627 (UMLS CUI [2,3])
C3843040 (UMLS CUI [3,1])
C0392760 (UMLS CUI [3,2])
C2348577 (UMLS CUI [3,3])
C0680082 (UMLS CUI [4,1])
C0392760 (UMLS CUI [4,2])
C3858758 (UMLS CUI [4,3])
C0681873 (UMLS CUI [4,4])
C0680082 (UMLS CUI [5,1])
C0392760 (UMLS CUI [5,2])
C2985627 (UMLS CUI [5,3])
C0680082 (UMLS CUI [6,1])
C0392760 (UMLS CUI [6,2])
C2348577 (UMLS CUI [6,3])