ID

14854

Description

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

Link

https://clinicaltrials.gov/show/NCT00026117

Keywords

  1. 5/1/16 5/1/16 -
  2. 6/26/16 6/26/16 -
  3. 6/26/16 6/26/16 -
Uploaded on

May 1, 2016

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Breast Cancer NCT00026117

Eligibility Breast Cancer NCT00026117

Criteria
Description

Criteria

breast or colorectal primary tumor sites
Description

ID.1

Data type

boolean

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

ID.2

Data type

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)
Description

ID.3

Data type

boolean

Alias
UMLS CUI [1]
C0392920
patient characteristics:
Description

ID.4

Data type

boolean

Alias
UMLS CUI [1]
C0815172
age:
Description

ID.5

Data type

boolean

Alias
UMLS CUI [1]
C0001779
18 and over
Description

ID.6

Data type

boolean

sex:
Description

ID.7

Data type

boolean

Alias
UMLS CUI [1]
C0079399
male or female
Description

ID.8

Data type

boolean

performance status:
Description

ID.9

Data type

boolean

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

ID.10

Data type

boolean

life expectancy:
Description

ID.11

Data type

boolean

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

ID.12

Data type

boolean

hepatic:
Description

ID.13

Data type

boolean

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

ID.14

Data type

boolean

renal:
Description

ID.15

Data type

boolean

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

ID.16

Data type

boolean

other:
Description

ID.17

Data type

boolean

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

ID.18

Data type

boolean

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

ID.19

Data type

boolean

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

ID.20

Data type

boolean

Alias
UMLS CUI [1]
C0009429
chemotherapy:
Description

ID.21

Data type

boolean

Alias
UMLS CUI [1]
C0392920
concurrent chemotherapy allowed
Description

ID.22

Data type

boolean

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

ID.23

Data type

boolean

Alias
UMLS CUI [1]
C2348568
other:
Description

ID.24

Data type

boolean

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

ID.25

Data type

boolean

Similar models

Eligibility Breast Cancer NCT00026117

Name
Type
Description | Question | Decode (Coded Value)
Data type
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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