ID

14854

Beskrivning

Shark Cartilage in Treating Patients With Advanced Colorectal or Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00026117

Länk

https://clinicaltrials.gov/show/NCT00026117

Nyckelord

  1. 2016-05-01 2016-05-01 -
  2. 2016-06-26 2016-06-26 -
  3. 2016-06-26 2016-06-26 -
Uppladdad den

1 maj 2016

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Breast Cancer NCT00026117

Eligibility Breast Cancer NCT00026117

Criteria
Beskrivning

Criteria

breast or colorectal primary tumor sites
Beskrivning

ID.1

Datatyp

boolean

Alias
UMLS CUI [1]
C0678222|C0009402
considered incurable
Beskrivning

ID.2

Datatyp

boolean

Alias
UMLS CUI [1]
C0175969
breast cancer patients must have disease progression after at least 2 different chemotherapy regimens (may include chemotherapy given as an adjuvant treatment)
Beskrivning

ID.3

Datatyp

boolean

Alias
UMLS CUI [1]
C0392920
patient characteristics:
Beskrivning

ID.4

Datatyp

boolean

Alias
UMLS CUI [1]
C0815172
age:
Beskrivning

ID.5

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
18 and over
Beskrivning

ID.6

Datatyp

boolean

sex:
Beskrivning

ID.7

Datatyp

boolean

Alias
UMLS CUI [1]
C0079399
male or female
Beskrivning

ID.8

Datatyp

boolean

performance status:
Beskrivning

ID.9

Datatyp

boolean

Alias
UMLS CUI [1]
C1520224
ecog 0-2
Beskrivning

ID.10

Datatyp

boolean

life expectancy:
Beskrivning

ID.11

Datatyp

boolean

Alias
UMLS CUI [1]
C0023671
more than 3 months
Beskrivning

ID.12

Datatyp

boolean

hepatic:
Beskrivning

ID.13

Datatyp

boolean

Alias
UMLS CUI [1]
C0205054
bilirubin no greater than 3 times upper limit of normal (uln)
Beskrivning

ID.14

Datatyp

boolean

renal:
Beskrivning

ID.15

Datatyp

boolean

Alias
UMLS CUI [1]
C0022646
calcium less than 1.2 times uln
Beskrivning

ID.16

Datatyp

boolean

other:
Beskrivning

ID.17

Datatyp

boolean

Alias
UMLS CUI [1]
C0205394
not pregnant or nursing
Beskrivning

ID.18

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
fertile patients must use effective contraception
Beskrivning

ID.19

Datatyp

boolean

Alias
UMLS CUI [1]
C0015895
prior concurrent therapy:
Beskrivning

ID.20

Datatyp

boolean

Alias
UMLS CUI [1]
C0009429
chemotherapy:
Beskrivning

ID.21

Datatyp

boolean

Alias
UMLS CUI [1]
C0392920
concurrent chemotherapy allowed
Beskrivning

ID.22

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0009429
no concurrent participation in a cytotoxic chemotherapy clinical trial
Beskrivning

ID.23

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
other:
Beskrivning

ID.24

Datatyp

boolean

Alias
UMLS CUI [1]
C0205394
at least 60 days since prior shark cartilage
Beskrivning

ID.25

Datatyp

boolean

Similar models

Eligibility Breast Cancer NCT00026117

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
ID.1
Item
breast or colorectal primary tumor sites
boolean
C0678222|C0009402 (UMLS CUI [1])
ID.2
Item
considered incurable
boolean
C0175969 (UMLS CUI [1])
ID.3
Item
breast cancer patients must have disease progression after at least 2 different chemotherapy regimens (may include chemotherapy given as an adjuvant treatment)
boolean
C0392920 (UMLS CUI [1])
ID.4
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
ID.5
Item
age:
boolean
C0001779 (UMLS CUI [1])
ID.6
Item
18 and over
boolean
ID.7
Item
sex:
boolean
C0079399 (UMLS CUI [1])
ID.8
Item
male or female
boolean
ID.9
Item
performance status:
boolean
C1520224 (UMLS CUI [1])
ID.10
Item
ecog 0-2
boolean
ID.11
Item
life expectancy:
boolean
C0023671 (UMLS CUI [1])
ID.12
Item
more than 3 months
boolean
ID.13
Item
hepatic:
boolean
C0205054 (UMLS CUI [1])
ID.14
Item
bilirubin no greater than 3 times upper limit of normal (uln)
boolean
ID.15
Item
renal:
boolean
C0022646 (UMLS CUI [1])
ID.16
Item
calcium less than 1.2 times uln
boolean
ID.17
Item
other:
boolean
C0205394 (UMLS CUI [1])
ID.18
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
ID.19
Item
fertile patients must use effective contraception
boolean
C0015895 (UMLS CUI [1])
ID.20
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
ID.21
Item
chemotherapy:
boolean
C0392920 (UMLS CUI [1])
ID.22
Item
concurrent chemotherapy allowed
boolean
C0392920 (UMLS CUI [1,1])
C0009429 (UMLS CUI [1,2])
ID.23
Item
no concurrent participation in a cytotoxic chemotherapy clinical trial
boolean
C2348568 (UMLS CUI [1])
ID.24
Item
other:
boolean
C0205394 (UMLS CUI [1])
ID.25
Item
at least 60 days since prior shark cartilage
boolean

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