Eligibility Prostate Cancer NCT01368055

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
prostate cancer.
Descrizione

ID.1

Tipo di dati

boolean

gleason score 2-6 or 7.
Descrizione

ID.2

Tipo di dati

boolean

psa ≤ 20 ng/ml.
Descrizione

ID.3

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous prostate cancer surgery or pelvic radiation.
Descrizione

ID.4

Tipo di dati

boolean

prior/concurrent systemic chemotherapy for prostate cancer.
Descrizione

ID.5

Tipo di dati

boolean

active inflammatory bowel disease (crohn's disease, diverticulitis or ulcerative colitis) affecting the rectum.
Descrizione

ID.6

Tipo di dati

boolean

history of hip replacement.
Descrizione

ID.7

Tipo di dati

boolean

prior intrapelvic surgery.
Descrizione

ID.8

Tipo di dati

boolean

taking saw palmetto or methotrexate and unable or unwilling to discontinue its uses during radiation.
Descrizione

ID.9

Tipo di dati

boolean

receiving continuous and current anticoagulation with warfarin sodium (coumadin), clopidogrel bisulfate (plavix), dabigatran etexilate mesylate (pradaxa),enoxaparin sodium (lovenox), or aspirin/er dipyridamole (aggrenox).
Descrizione

ID.10

Tipo di dati

boolean

Similar models

Eligibility Prostate Cancer NCT01368055

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
prostate cancer.
boolean
ID.2
Item
gleason score 2-6 or 7.
boolean
ID.3
Item
psa ≤ 20 ng/ml.
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
previous prostate cancer surgery or pelvic radiation.
boolean
ID.5
Item
prior/concurrent systemic chemotherapy for prostate cancer.
boolean
ID.6
Item
active inflammatory bowel disease (crohn's disease, diverticulitis or ulcerative colitis) affecting the rectum.
boolean
ID.7
Item
history of hip replacement.
boolean
ID.8
Item
prior intrapelvic surgery.
boolean
ID.9
Item
taking saw palmetto or methotrexate and unable or unwilling to discontinue its uses during radiation.
boolean
ID.10
Item
receiving continuous and current anticoagulation with warfarin sodium (coumadin), clopidogrel bisulfate (plavix), dabigatran etexilate mesylate (pradaxa),enoxaparin sodium (lovenox), or aspirin/er dipyridamole (aggrenox).
boolean