Informed Consent
Item
informed consent to participate in study.
boolean
C0021430 (UMLS CUI [1])
Biopsy of prostate Negative Single
Item
have had a single negative prostate biopsy within 6 months prior to enrollment in study.
boolean
C0194804 (UMLS CUI [1,1])
C1513916 (UMLS CUI [1,2])
C0205171 (UMLS CUI [1,3])
Prostate-Specific Antigen | Age
Item
have a psa (prostate specific antigen) between 2.5 and 10 if 50-60 years of age; or a psa between 3.0 and 10 if over age 60.
boolean
C0138741 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Study Subject Participation Status Duration
Item
ability and will to participate in study for 4 years.
boolean
C2348568 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Biopsy of prostate Negative Quantity
Item
more than one previous negative prostate biopsy.
boolean
C0194804 (UMLS CUI [1,1])
C1513916 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Prostate carcinoma
Item
history of prostate cancer.
boolean
C0600139 (UMLS CUI [1])
Operation on prostate
Item
previous prostate surgery.
boolean
C0194790 (UMLS CUI [1])
Unable to urinate | Catheter Patient need for
Item
inability to urinate requiring the need of a catheter during the previous 2 years.
boolean
C0849752 (UMLS CUI [1])
C0085590 (UMLS CUI [2,1])
C0686904 (UMLS CUI [2,2])
Condition Resulting in Urinary symptoms | Condition Resulting in Urine Flow Rate Change | Benign prostatic hypertrophy
Item
any condition (other than benign prostatic hypertrophy) which may result in urinary symptoms or changes in urine flow rate.
boolean
C0348080 (UMLS CUI [1,1])
C0332294 (UMLS CUI [1,2])
C0426359 (UMLS CUI [1,3])
C0348080 (UMLS CUI [2,1])
C0332294 (UMLS CUI [2,2])
C0042036 (UMLS CUI [2,3])
C2826285 (UMLS CUI [2,4])
C0392747 (UMLS CUI [2,5])
C1704272 (UMLS CUI [3])
Malignant Neoplasms | Basal cell carcinoma | Squamous cell carcinoma of skin
Item
cancer within previous 5 years (other than basal or squamous cell cancers of the skin).
boolean
C0006826 (UMLS CUI [1])
C0007117 (UMLS CUI [2])
C0553723 (UMLS CUI [3])
Medical condition Serious Unstable
Item
any unstable serious medical condition.
boolean
C3843040 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0443343 (UMLS CUI [1,3])
Finasteride | Proscar | Propecia | Dutasteride | Avodart | Testosterone | Androgen Antagonists
Item
use within the past 12 months of finasteride (proscar or propecia), dutasteride (avodart), testosterone, or drugs that can block the action of male hormones.
boolean
C0060389 (UMLS CUI [1])
C0678149 (UMLS CUI [2])
C0722858 (UMLS CUI [3])
C0754659 (UMLS CUI [4])
C1170079 (UMLS CUI [5])
C0039601 (UMLS CUI [6])
C0002842 (UMLS CUI [7])