Standard of Care Prostatectomy Scheduled | Prostate carcinoma Localized Presumptive
Item
participant must be scheduled to undergo standard of care prostatectomy for presumed localized prostate cancer at the national institutes of health (nih) clinical center.
boolean
C2936643 (UMLS CUI [1,1])
C0033573 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
C0600139 (UMLS CUI [2,1])
C0392752 (UMLS CUI [2,2])
C3640893 (UMLS CUI [2,3])
Adenocarcinoma of prostate Transrectal biopsy | Adenocarcinoma of prostate Sextant biopsy
Item
recent (within 12 months of study entry) trans-rectal biopsy indicating the presence of adenocarcinoma of the prostate gland in which at least sextant biopsies were obtained. knowledge of the location of each specimen is required for inclusion.
boolean
C0007112 (UMLS CUI [1,1])
C0401641 (UMLS CUI [1,2])
C0007112 (UMLS CUI [2,1])
C3846092 (UMLS CUI [2,2])
Age
Item
participant must be 18 years or older.
boolean
C0001779 (UMLS CUI [1])
Serum creatinine measurement prior to Magnetic Resonance Imaging | Epidermal Growth Factor Receptor Measurement
Item
serum creatinine within 1 week prior to magnetic resonance (mr) imaging less than or equal to 1.8mg/dl and epidermal growth factor receptor (egfr) must be greater than 30 ml/min/1.73 m^2
boolean
C0201976 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
C0024485 (UMLS CUI [1,3])
C3812682 (UMLS CUI [2])
ECOG performance status
Item
eastern cooperative oncology group (ecog) performance score of 0 or 1.
boolean
C1520224 (UMLS CUI [1])
Informed Consent
Item
ability to provide informed consent. all patients must sign a document of informed consent indicating their understanding of the investigational nature and risks of the study before any protocol related studies are performed.
boolean
C0021430 (UMLS CUI [1])
Hypersensitivity Gadolinium | Hypersensitivity Acetate
Item
known allergy to gadolinium or acetate.
boolean
C0020517 (UMLS CUI [1,1])
C0016911 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0000975 (UMLS CUI [2,2])
Study Subject Participation Status Causing Delay Standard of Care
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])
Comorbidity Interferes with Study procedure | Mental condition Interferes with Study procedure | Comorbidity Interferes with Research results | Mental condition Interferes with Research results
Item
participants with any coexisting medical or psychiatric condition that is likely to interfere with study procedures and/or results are excluded.
boolean
C0009488 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C2603343 (UMLS CUI [1,3])
C0184661 (UMLS CUI [1,4])
C3840291 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C2603343 (UMLS CUI [2,3])
C0184661 (UMLS CUI [2,4])
C0009488 (UMLS CUI [3,1])
C0521102 (UMLS CUI [3,2])
C0683954 (UMLS CUI [3,3])
C3840291 (UMLS CUI [4,1])
C0521102 (UMLS CUI [4,2])
C0683954 (UMLS CUI [4,3])
Claustrophobia Severe
Item
participants with severe claustrophobia.
boolean
C0008909 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Medical contraindication Magnetic Resonance Imaging
Item
patients with contraindications to magnetic resonance imaging (mri)
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
Body Weight
Item
patients weighing greater than 136 kg (weight limit for scanner table).
boolean
C0005910 (UMLS CUI [1])
Artificial cardiac pacemaker | Aneurysm clip cerebral | Shrapnel injury | Implants Electronic Inconsistent MRI | Metal Inconsistent MRI
Item
patients with pacemakers, cerebral aneurysm clips, shrapnel injury, or other implanted electronic devices or metal not compatible with mri.
boolean
C0030163 (UMLS CUI [1])
C0179977 (UMLS CUI [2,1])
C0006104 (UMLS CUI [2,2])
C0522670 (UMLS CUI [3,1])
C3263723 (UMLS CUI [3,2])
C0021102 (UMLS CUI [4,1])
C0013850 (UMLS CUI [4,2])
C0442809 (UMLS CUI [4,3])
C0024485 (UMLS CUI [4,4])
C0025552 (UMLS CUI [5,1])
C0442809 (UMLS CUI [5,2])
C0024485 (UMLS CUI [5,3])
Medical contraindication Placement Coil Endorectal
Item
patients with contraindication to endorectal coil placement
boolean
C1301624 (UMLS CUI [1,1])
C0441587 (UMLS CUI [1,2])
C1705946 (UMLS CUI [1,3])
C0524447 (UMLS CUI [1,4])
Hemorrhoids Severe
Item
severe hemorrhoids.
boolean
C0019112 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Rectum Absent Surgical
Item
surgically absent rectum.
boolean
C0034896 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0543467 (UMLS CUI [1,3])
Other medical condition Study Subject Participation Status Ineligible
Item
other medical conditions deemed by the principal investigator (pi) or associates to make the patient ineligible for protocol procedures.
boolean
C3843040 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C1512714 (UMLS CUI [1,3])
Radiotherapy to pelvis
Item
patients who have previously received radiation therapy to the pelvis.
boolean
C1536155 (UMLS CUI [1])
Antiandrogen therapy
Item
patients who have received androgen deprivation therapy.
boolean
C0279492 (UMLS CUI [1])