ID

22523

Beschrijving

Selenium in Treating Patients Who Are Undergoing Brachytherapy for Stage I or Stage II Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00217516

Link

https://clinicaltrials.gov/show/NCT00217516

Trefwoorden

Versies (2)
  1. 06-06-17 06-06-17 -
  2. 07-06-17 07-06-17 -
Geüploaded op

6 juni 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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Eligibility Prostate Cancer NCT00217516

Engels

Eligibility Prostate Cancer NCT00217516

1 Formulieren  
Criteria
Beschrijving

Criteria

histologically confirmed adenocarcinoma of the prostate
Beschrijving

Adenocarcinoma of prostate

Datatype

boolean

Alias
UMLS CUI [1]
C0007112
must have undergone ≥ a sextant biopsy
Beschrijving

Sextant biopsy Quantity

Datatype

boolean

Alias
UMLS CUI [1,1]
C3846092
UMLS CUI [1,2]
C1265611
clinical stage t1a-t2a disease
Beschrijving

TNM clinical staging

Datatype

boolean

Alias
UMLS CUI [1]
C3258246
gleason score < 8
Beschrijving

Gleason score

Datatype

boolean

Alias
UMLS CUI [1]
C3203027
prostate-specific antigen < 20 ng/ml
Beschrijving

Prostate specific antigen measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0201544
patient characteristics:
Beschrijving

Client Characteristics

Datatype

boolean

Alias
UMLS CUI [1]
C0815172
not specified
Beschrijving

Unspecified

Datatype

boolean

Alias
UMLS CUI [1]
C0205370
performance status
Beschrijving

performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1518965
not specified
Beschrijving

Unspecified

Datatype

boolean

Alias
UMLS CUI [1]
C0205370
life expectancy
Beschrijving

Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
more than 5 years
Beschrijving

Year Quantity

Datatype

boolean

Alias
UMLS CUI [1,1]
C0439234
UMLS CUI [1,2]
C1265611
hematopoietic
Beschrijving

Function Hematopoietic

Datatype

boolean

Alias
UMLS CUI [1,1]
C0031843
UMLS CUI [1,2]
C0229601
not specified
Beschrijving

Unspecified

Datatype

boolean

Alias
UMLS CUI [1]
C0205370
hepatic
Beschrijving

Liver function

Datatype

boolean

Alias
UMLS CUI [1]
C0232741
not specified
Beschrijving

Unspecified

Datatype

boolean

Alias
UMLS CUI [1]
C0205370
renal
Beschrijving

Renal function

Datatype

boolean

Alias
UMLS CUI [1]
C0232804
not specified
Beschrijving

Unspecified

Datatype

boolean

Alias
UMLS CUI [1]
C0205370
other
Beschrijving

Client Characteristics

Datatype

boolean

Alias
UMLS CUI [1]
C0815172
no other prior malignancy except nonmelanoma skin cancer
Beschrijving

Malignant Neoplasms | Skin carcinoma

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0699893
prior concurrent therapy:
Beschrijving

Therapeutic procedure

Datatype

boolean

Alias
UMLS CUI [1]
C0087111
biologic therapy
Beschrijving

Biological treatment

Datatype

boolean

Alias
UMLS CUI [1]
C1531518
not specified
Beschrijving

Unspecified

Datatype

boolean

Alias
UMLS CUI [1]
C0205370
chemotherapy
Beschrijving

Chemotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C0392920
not specified
Beschrijving

Unspecified

Datatype

boolean

Alias
UMLS CUI [1]
C0205370
endocrine therapy
Beschrijving

Hormone Therapy

Datatype

boolean

Alias
UMLS CUI [1]
C0279025
no prior hormonal therapy
Beschrijving

Prior Hormone Therapy Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C1514460
UMLS CUI [1,2]
C0332197
radiotherapy
Beschrijving

Therapeutic radiology procedure

Datatype

boolean

Alias
UMLS CUI [1]
C1522449
no prior radiotherapy
Beschrijving

Prior radiation therapy Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0279134
UMLS CUI [1,2]
C0332197
surgery
Beschrijving

Operative Surgical Procedures

Datatype

boolean

Alias
UMLS CUI [1]
C0543467
not specified
Beschrijving

Unspecified

Datatype

boolean

Alias
UMLS CUI [1]
C0205370
other
Beschrijving

Therapeutic procedure

Datatype

boolean

Alias
UMLS CUI [1]
C0087111
more than 30 days since prior and no concurrent participation in another clinical trial involving a medical, surgical, nutritional, or lifestyle intervention (e.g., dietary modification or exercise)
Beschrijving

Study Subject Participation Status | Interventional procedure | Operative Surgical Procedures | Nutritional Intervention | Life Style Interventional procedure | Dietary Modification | Exercise

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0184661
UMLS CUI [3]
C0543467
UMLS CUI [4]
C1882127
UMLS CUI [5,1]
C0023676
UMLS CUI [5,2]
C0184661
UMLS CUI [6]
C0086153
UMLS CUI [7]
C0015259
no selenium at doses > 50 mcg/day as a dietary supplement, including multivitamin supplements
Beschrijving

Selenium Dose U/day | Dietary Supplement | Multivitamin preparation Supplement

Datatype

boolean

Alias
UMLS CUI [1,1]
C0036581
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0456683
UMLS CUI [2]
C0242295
UMLS CUI [3,1]
C0301532
UMLS CUI [3,2]
C2348609
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Similar models

Eligibility Prostate Cancer NCT00217516

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Adenocarcinoma of prostate
Item
histologically confirmed adenocarcinoma of the prostate
boolean
C0007112 (UMLS CUI [1])
Sextant biopsy Quantity
Item
must have undergone ≥ a sextant biopsy
boolean
C3846092 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
TNM clinical staging
Item
clinical stage t1a-t2a disease
boolean
C3258246 (UMLS CUI [1])
Gleason score
Item
gleason score < 8
boolean
C3203027 (UMLS CUI [1])
Prostate specific antigen measurement
Item
prostate-specific antigen < 20 ng/ml
boolean
C0201544 (UMLS CUI [1])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
performance status
Item
performance status
boolean
C1518965 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Life Expectancy
Item
life expectancy
boolean
C0023671 (UMLS CUI [1])
Year Quantity
Item
more than 5 years
boolean
C0439234 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Function Hematopoietic
Item
hematopoietic
boolean
C0031843 (UMLS CUI [1,1])
C0229601 (UMLS CUI [1,2])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Liver function
Item
hepatic
boolean
C0232741 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Renal function
Item
renal
boolean
C0232804 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Client Characteristics
Item
other
boolean
C0815172 (UMLS CUI [1])
Malignant Neoplasms | Skin carcinoma
Item
no other prior malignancy except nonmelanoma skin cancer
boolean
C0006826 (UMLS CUI [1])
C0699893 (UMLS CUI [2])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Biological treatment
Item
biologic therapy
boolean
C1531518 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Chemotherapy
Item
chemotherapy
boolean
C0392920 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Hormone Therapy
Item
endocrine therapy
boolean
C0279025 (UMLS CUI [1])
Prior Hormone Therapy Absent
Item
no prior hormonal therapy
boolean
C1514460 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Therapeutic radiology procedure
Item
radiotherapy
boolean
C1522449 (UMLS CUI [1])
Prior radiation therapy Absent
Item
no prior radiotherapy
boolean
C0279134 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Operative Surgical Procedures
Item
surgery
boolean
C0543467 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Therapeutic procedure
Item
other
boolean
C0087111 (UMLS CUI [1])
Study Subject Participation Status | Interventional procedure | Operative Surgical Procedures | Nutritional Intervention | Life Style Interventional procedure | Dietary Modification | Exercise
Item
more than 30 days since prior and no concurrent participation in another clinical trial involving a medical, surgical, nutritional, or lifestyle intervention (e.g., dietary modification or exercise)
boolean
C2348568 (UMLS CUI [1])
C0184661 (UMLS CUI [2])
C0543467 (UMLS CUI [3])
C1882127 (UMLS CUI [4])
C0023676 (UMLS CUI [5,1])
C0184661 (UMLS CUI [5,2])
C0086153 (UMLS CUI [6])
C0015259 (UMLS CUI [7])
Selenium Dose U/day | Dietary Supplement | Multivitamin preparation Supplement
Item
no selenium at doses > 50 mcg/day as a dietary supplement, including multivitamin supplements
boolean
C0036581 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0456683 (UMLS CUI [1,3])
C0242295 (UMLS CUI [2])
C0301532 (UMLS CUI [3,1])
C2348609 (UMLS CUI [3,2])
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