ID

18913

Description

Pomegranate Juice in Treating Patients With Recurrent Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00060086

Link

https://clinicaltrials.gov/show/NCT00060086

Keywords

  1. 11/24/16 11/24/16 -
Uploaded on

November 24, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT00060086

Eligibility Prostate Cancer NCT00060086

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed adenocarcinoma of the prostate
Description

Adenocarcinoma of prostate

Data type

boolean

Alias
UMLS CUI [1]
C0007112
must have undergone prior surgery or radiotherapy for the primary tumor
Description

Prior surgery primary tumor | prior radiation therapy primary tumor

Data type

boolean

Alias
UMLS CUI [1,1]
C0455610
UMLS CUI [1,2]
C0677930
UMLS CUI [2,1]
C0279134
UMLS CUI [2,2]
C0677930
documented rising prostate-specific antigen (psa) level, defined by the following criteria:
Description

Raised prostate specific antigen

Data type

boolean

Alias
UMLS CUI [1]
C0178415
absolute level of psa at least 0.2 ng/ml but less than 5.0 ng/ml
Description

Prostate specific antigen measurement Absolute

Data type

boolean

Alias
UMLS CUI [1,1]
C0201544
UMLS CUI [1,2]
C0205344
rising psa level must be confirmed at least 1 week later
Description

Raised prostate specific antigen Confirmation Point in time

Data type

boolean

Alias
UMLS CUI [1,1]
C0178415
UMLS CUI [1,2]
C0750484
UMLS CUI [1,3]
C1442880
adequate psa time points to calculate a psa doubling time
Description

Prostate-Specific Antigen measurement Point in time Quantity | Calculation Prostate-Specific Antigen Doubling Time

Data type

boolean

Alias
UMLS CUI [1,1]
C0201544
UMLS CUI [1,2]
C1442880
UMLS CUI [1,3]
C1265611
UMLS CUI [2,1]
C1441506
UMLS CUI [2,2]
C0138741
UMLS CUI [2,3]
C1705764
UMLS CUI [2,4]
C0040223
gleason score no greater than 7
Description

Gleason score

Data type

boolean

Alias
UMLS CUI [1]
C3203027
age 18 and over
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
performance status ecog 0-1
Description

ECOG performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
life expectancy at least 6 months
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
no other malignancy within the past 5 years except nonmelanoma skin cancer
Description

Malignant Neoplasms | Skin carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0699893
no other serious concurrent systemic medical disorders that would preclude study compliance
Description

Systemic disease Serious Excludes Protocol Compliance

Data type

boolean

Alias
UMLS CUI [1,1]
C0442893
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C0332196
UMLS CUI [1,4]
C0525058
no known allergy to pomegranate juice
Description

Hypersensitivity POMEGRANATE JUICE

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1327962
more than 4 weeks since prior participation in another experimental study
Description

Study Subject Participation Status Previous

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0205156
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
nodal involvement
Description

nodal involvement

Data type

boolean

Alias
UMLS CUI [1]
C0441949
evidence of metastatic disease
Description

Neoplasm Metastasis Evidence of

Data type

boolean

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0332120
prior hormonal therapy
Description

Prior Hormone Therapy

Data type

boolean

Alias
UMLS CUI [1]
C1514460
concurrent hormonal therapy for rising psa levels after initial therapy for prostate cancer
Description

Therapeutic procedure Initial Prostate carcinoma | Hormone Therapy Raised prostate specific antigen

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0205265
UMLS CUI [1,3]
C0600139
UMLS CUI [2,1]
C0279025
UMLS CUI [2,2]
C0178415
concurrent participation in another experimental study
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
other concurrent systemic or local therapy for prostate cancer
Description

systemic therapy Prostate carcinoma | Local Therapy Prostate carcinoma

Data type

boolean

Alias
UMLS CUI [1,1]
C1515119
UMLS CUI [1,2]
C0600139
UMLS CUI [2,1]
C1517925
UMLS CUI [2,2]
C0600139
initiation or discontinuation of any new nutritional or dietary supplements during study participation
Description

Initiation Nutritional Supplements New | Discontinuation Nutritional Supplements New

Data type

boolean

Alias
UMLS CUI [1,1]
C1704686
UMLS CUI [1,2]
C0242295
UMLS CUI [1,3]
C0205314
UMLS CUI [2,1]
C0457454
UMLS CUI [2,2]
C0242295
UMLS CUI [2,3]
C0205314

Similar models

Eligibility Prostate Cancer NCT00060086

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Adenocarcinoma of prostate
Item
histologically confirmed adenocarcinoma of the prostate
boolean
C0007112 (UMLS CUI [1])
Prior surgery primary tumor | prior radiation therapy primary tumor
Item
must have undergone prior surgery or radiotherapy for the primary tumor
boolean
C0455610 (UMLS CUI [1,1])
C0677930 (UMLS CUI [1,2])
C0279134 (UMLS CUI [2,1])
C0677930 (UMLS CUI [2,2])
Raised prostate specific antigen
Item
documented rising prostate-specific antigen (psa) level, defined by the following criteria:
boolean
C0178415 (UMLS CUI [1])
Prostate specific antigen measurement Absolute
Item
absolute level of psa at least 0.2 ng/ml but less than 5.0 ng/ml
boolean
C0201544 (UMLS CUI [1,1])
C0205344 (UMLS CUI [1,2])
Raised prostate specific antigen Confirmation Point in time
Item
rising psa level must be confirmed at least 1 week later
boolean
C0178415 (UMLS CUI [1,1])
C0750484 (UMLS CUI [1,2])
C1442880 (UMLS CUI [1,3])
Prostate-Specific Antigen measurement Point in time Quantity | Calculation Prostate-Specific Antigen Doubling Time
Item
adequate psa time points to calculate a psa doubling time
boolean
C0201544 (UMLS CUI [1,1])
C1442880 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C1441506 (UMLS CUI [2,1])
C0138741 (UMLS CUI [2,2])
C1705764 (UMLS CUI [2,3])
C0040223 (UMLS CUI [2,4])
Gleason score
Item
gleason score no greater than 7
boolean
C3203027 (UMLS CUI [1])
Age
Item
age 18 and over
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
performance status ecog 0-1
boolean
C1520224 (UMLS CUI [1])
Life Expectancy
Item
life expectancy at least 6 months
boolean
C0023671 (UMLS CUI [1])
Malignant Neoplasms | Skin carcinoma
Item
no other malignancy within the past 5 years except nonmelanoma skin cancer
boolean
C0006826 (UMLS CUI [1])
C0699893 (UMLS CUI [2])
Systemic disease Serious Excludes Protocol Compliance
Item
no other serious concurrent systemic medical disorders that would preclude study compliance
boolean
C0442893 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0332196 (UMLS CUI [1,3])
C0525058 (UMLS CUI [1,4])
Hypersensitivity POMEGRANATE JUICE
Item
no known allergy to pomegranate juice
boolean
C0020517 (UMLS CUI [1,1])
C1327962 (UMLS CUI [1,2])
Study Subject Participation Status Previous
Item
more than 4 weeks since prior participation in another experimental study
boolean
C2348568 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
nodal involvement
Item
nodal involvement
boolean
C0441949 (UMLS CUI [1])
Neoplasm Metastasis Evidence of
Item
evidence of metastatic disease
boolean
C0027627 (UMLS CUI [1,1])
C0332120 (UMLS CUI [1,2])
Prior Hormone Therapy
Item
prior hormonal therapy
boolean
C1514460 (UMLS CUI [1])
Therapeutic procedure Initial Prostate carcinoma | Hormone Therapy Raised prostate specific antigen
Item
concurrent hormonal therapy for rising psa levels after initial therapy for prostate cancer
boolean
C0087111 (UMLS CUI [1,1])
C0205265 (UMLS CUI [1,2])
C0600139 (UMLS CUI [1,3])
C0279025 (UMLS CUI [2,1])
C0178415 (UMLS CUI [2,2])
Study Subject Participation Status
Item
concurrent participation in another experimental study
boolean
C2348568 (UMLS CUI [1])
systemic therapy Prostate carcinoma | Local Therapy Prostate carcinoma
Item
other concurrent systemic or local therapy for prostate cancer
boolean
C1515119 (UMLS CUI [1,1])
C0600139 (UMLS CUI [1,2])
C1517925 (UMLS CUI [2,1])
C0600139 (UMLS CUI [2,2])
Initiation Nutritional Supplements New | Discontinuation Nutritional Supplements New
Item
initiation or discontinuation of any new nutritional or dietary supplements during study participation
boolean
C1704686 (UMLS CUI [1,1])
C0242295 (UMLS CUI [1,2])
C0205314 (UMLS CUI [1,3])
C0457454 (UMLS CUI [2,1])
C0242295 (UMLS CUI [2,2])
C0205314 (UMLS CUI [2,3])

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