ID

34244

Beschrijving

Changes in Brown Adipose Tissue Activity In Men Receiving Androgen Deprivation Therapy for Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01226888

Link

https://clinicaltrials.gov/show/NCT01226888

Trefwoorden

  1. 15-01-19 15-01-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

15 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT01226888

Eligibility Prostate Cancer NCT01226888

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
adenocarcinoma of the prostate
Beschrijving

Adenocarcinoma of prostate

Datatype

boolean

Alias
UMLS CUI [1]
C0007112
scheduled to initiate gnrh agonist or antagonist treatment with an intended treatment duration of 12 months or greater
Beschrijving

GnRH Agonist Scheduled | GnRH antagonist Scheduled

Datatype

boolean

Alias
UMLS CUI [1,1]
C2267073
UMLS CUI [1,2]
C0205539
UMLS CUI [2,1]
C1268855
UMLS CUI [2,2]
C0205539
ecog performance status of 0 or 1
Beschrijving

ECOG performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
ability to understand and the willingness to sign a written informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
65 years of age or younger
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
diagnosis of diabetes
Beschrijving

Diabetes Mellitus

Datatype

boolean

Alias
UMLS CUI [1]
C0011849
ongoing corticosteroid use
Beschrijving

Adrenal Cortex Hormones

Datatype

boolean

Alias
UMLS CUI [1]
C0001617
gnrh agonist or antagonist treatment within the last 2 years
Beschrijving

GnRH Agonist | GnRH antagonist

Datatype

boolean

Alias
UMLS CUI [1]
C2267073
UMLS CUI [2]
C1268855
ongoing beta-blocker use
Beschrijving

Adrenergic beta-1 Receptor Antagonists

Datatype

boolean

Alias
UMLS CUI [1]
C0304516
body mass index of greater than 30
Beschrijving

Body mass index

Datatype

boolean

Alias
UMLS CUI [1]
C1305855

Similar models

Eligibility Prostate Cancer NCT01226888

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Adenocarcinoma of prostate
Item
adenocarcinoma of the prostate
boolean
C0007112 (UMLS CUI [1])
GnRH Agonist Scheduled | GnRH antagonist Scheduled
Item
scheduled to initiate gnrh agonist or antagonist treatment with an intended treatment duration of 12 months or greater
boolean
C2267073 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
C1268855 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
ECOG performance status
Item
ecog performance status of 0 or 1
boolean
C1520224 (UMLS CUI [1])
Informed Consent
Item
ability to understand and the willingness to sign a written informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
65 years of age or younger
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Diabetes Mellitus
Item
diagnosis of diabetes
boolean
C0011849 (UMLS CUI [1])
Adrenal Cortex Hormones
Item
ongoing corticosteroid use
boolean
C0001617 (UMLS CUI [1])
GnRH Agonist | GnRH antagonist
Item
gnrh agonist or antagonist treatment within the last 2 years
boolean
C2267073 (UMLS CUI [1])
C1268855 (UMLS CUI [2])
Adrenergic beta-1 Receptor Antagonists
Item
ongoing beta-blocker use
boolean
C0304516 (UMLS CUI [1])
Body mass index
Item
body mass index of greater than 30
boolean
C1305855 (UMLS CUI [1])

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