Age
Item
18 years of age or older
boolean
C0001779 (UMLS CUI [1])
Prostate carcinoma
Item
histologically proven prostate cancer
boolean
C0600139 (UMLS CUI [1])
Treatment Plan Antiandrogen therapy Long-term
Item
treatment plan is to administer long term adt (androgen deprivation therapy).
boolean
C0599880 (UMLS CUI [1,1])
C0279492 (UMLS CUI [1,2])
C0443252 (UMLS CUI [1,3])
Antiandrogen therapy | Combined Modality Therapy | Androgen Antagonists | LHRH Analogs | Androgen Antagonists Alone Excluded
Item
patient must currently be treated with adt for at least 2 weeks before enrollment in trial, and for no more than 6 months. patient treated with a maximum androgen blockade strategy, combining an anti-androgen agent with a lhrh analog agent are admissible to this protocol, but not patients treated only with an anti-androgen agent alone.
boolean
C0279492 (UMLS CUI [1])
C0009429 (UMLS CUI [2])
C0002842 (UMLS CUI [3])
C1518041 (UMLS CUI [4])
C0002842 (UMLS CUI [5,1])
C0205171 (UMLS CUI [5,2])
C0332196 (UMLS CUI [5,3])
Informed Consent
Item
written informed consent to participate in the trial.
boolean
C0021430 (UMLS CUI [1])
Hypersensitivity Zoladex | Hypersensitivity Casodex | Hypersensitivity Zoladex Component | Hypersensitivity Casodex Component | Hypersensitivity Pharmaceutical Preparations Similar
Item
known hypersensitivity to zoladex, casodex (if applicable), or any component of these product, or to other similar agents
boolean
C0020517 (UMLS CUI [1,1])
C0149473 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0591237 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0149473 (UMLS CUI [3,2])
C1705248 (UMLS CUI [3,3])
C0020517 (UMLS CUI [4,1])
C0591237 (UMLS CUI [4,2])
C1705248 (UMLS CUI [4,3])
C0020517 (UMLS CUI [5,1])
C0013227 (UMLS CUI [5,2])
C2348205 (UMLS CUI [5,3])
Heart Disease Severe New York Heart Association Classification
Item
severe cardiac disease (new york heart association class iii or greater)
boolean
C0018799 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,3])
Lung disease Severe
Item
severe lung disease
boolean
C0024115 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Uncontrolled pain
Item
uncontrollable pain
boolean
C0747149 (UMLS CUI [1])
Bone lesion Unstable
Item
unstable bone lesion
boolean
C0238792 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
Comorbidity Difficulty walking | Modification Walking habits Limited | Parkinson Disease | Multiple Sclerosis Advanced | Amputation of lower limb
Item
any co-morbidity restraining the patient's ability to walk alone or to modify his walking habits (eg parkinson's disease, advanced multiple sclerosis, leg amputation, ...)
boolean
C0009488 (UMLS CUI [1,1])
C0311394 (UMLS CUI [1,2])
C3840684 (UMLS CUI [2,1])
C0080331 (UMLS CUI [2,2])
C2242848 (UMLS CUI [2,3])
C0439801 (UMLS CUI [2,4])
C0030567 (UMLS CUI [3])
C0026769 (UMLS CUI [4,1])
C0205179 (UMLS CUI [4,2])
C0337308 (UMLS CUI [5])
Comorbidity Study Subject Participation Status Unfavorable | Comorbidity compromises Protocol Compliance
Item
any concomitant condition that would make it undesirable, in the physician's opinion, for the subject to participate in the trial or would jeopardize compliance with the protocol.
boolean
C0009488 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C3640815 (UMLS CUI [1,3])
C0009488 (UMLS CUI [2,1])
C2945640 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
Medical contraindication 6-Minute Walk Test | Angina, Unstable | Myocardial Infarction | Resting heart rate | Increased systolic pressure | Increased diastolic pressure | Cardiovascular conditions Stabilized Controlled
Item
any contraindication to undertake the 6-minutes walk test (unstable angina or myocardial infarction during the previous month, a resting heart rate of more than 180, systolic blood pressure of more than 180, and a diastolic pressure of more than 100). the patient must have his cardiovascular conditions stabilized and controlled before enrollment in the trial.
boolean
C1301624 (UMLS CUI [1,1])
C0430515 (UMLS CUI [1,2])
C0002965 (UMLS CUI [2])
C0027051 (UMLS CUI [3])
C1821417 (UMLS CUI [4])
C0277884 (UMLS CUI [5])
C0277889 (UMLS CUI [6])
C2015790 (UMLS CUI [7,1])
C0184512 (UMLS CUI [7,2])
C2911690 (UMLS CUI [7,3])
Informed Consent Unwilling | Informed Consent Unable
Item
unwillingness or incapacity to consent to trial participation.
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])