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ID
15860
Beschrijving
Micro RNAs to Predict Response to Androgen Deprivation Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT02366494
Link
https://clinicaltrials.gov/show/NCT02366494
Trefwoorden
Versies (1)
- 16-06-16 16-06-16 -
Geüploaded op
16 juni 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Prostate Cancer NCT02366494
Eligibility Prostate Cancer NCT02366494
- StudyEvent: Eligibility
Similar models
Eligibility Prostate Cancer NCT02366494
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
prostate cancer
Item
histologically proven prostate cancer.
boolean
C0600139 (UMLS CUI [1])
Testosterone measurement | Hormone Therapy
Item
testosterone level >30ng/ml and at least 6 months since last dose of hormonal therapy.
boolean
C0523912 (UMLS CUI [1])
C0279025 (UMLS CUI [2])
C0279025 (UMLS CUI [2])
Physical Examination | Prostate carcinoma | TNM clinical staging
Item
history/physical examination including a detailed description of the stage of prostate cancer within 8 weeks prior to registration.
boolean
C0031809 (UMLS CUI [1])
C0600139 (UMLS CUI [2])
C3258246 (UMLS CUI [3])
C0600139 (UMLS CUI [2])
C3258246 (UMLS CUI [3])
CT with intravenous contrast Abdomen | CT with intravenous contrast Pelvis | Radioisotope scan of bone
Item
ct scan of abdomen and pelvis with iv contrast and bone scan should be performed within 8 weeks prior to registration.
boolean
C0202653 (UMLS CUI [1,1])
C0000726 (UMLS CUI [1,2])
C0202653 (UMLS CUI [2,1])
C0030797 (UMLS CUI [2,2])
C0203668 (UMLS CUI [3])
C0000726 (UMLS CUI [1,2])
C0202653 (UMLS CUI [2,1])
C0030797 (UMLS CUI [2,2])
C0203668 (UMLS CUI [3])
ECOG performance status
Item
ecog performance status 0-2.
boolean
C1520224 (UMLS CUI [1])
Age
Item
age ≥ 18.
boolean
C0001779 (UMLS CUI [1])
Informed Consent | Blood specimen Requirement | BLOOD BANKING | Genetic testing
Item
patients must provide study-specific informed consent prior to study entry for this project and mandatory blood specimen for banking for future studies (future studies may include genetic testing).
boolean
C0021430 (UMLS CUI [1])
C0178913 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0200495 (UMLS CUI [3])
C0679560 (UMLS CUI [4])
C0178913 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0200495 (UMLS CUI [3])
C0679560 (UMLS CUI [4])
Hormone Therapy
Item
received hormonal therapy less than 6 months prior to registration.
boolean
C0279025 (UMLS CUI [1])
Secondary Malignant Neoplasm
Item
history of active secondary malignancy.
boolean
C3266877 (UMLS CUI [1])
Prostate carcinoma | Hormone Therapy Refused
Item
decline hormone therapy for prostate cancer.
boolean
C0600139 (UMLS CUI [1])
C0279025 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
C0279025 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Therapeutic procedure 5-alpha Reductase Inhibitors
Item
current or previous treatment with 5-alpha reductase inhibitors within 6 months prior to enrollment.
boolean
C0087111 (UMLS CUI [1,1])
C2936788 (UMLS CUI [1,2])
C2936788 (UMLS CUI [1,2])