ID

16015

Descripción

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

Palabras clave

  1. 1/5/16 1/5/16 -
  2. 26/6/16 26/6/16 -
  3. 26/6/16 26/6/16 -
Subido en

26 de junio de 2016

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00026117

Eligibility Breast Cancer NCT00026117

Criteria
Descripción

Criteria

breast or colorectal primary tumor sites
Descripción

breast or colorectal primary tumor

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0678222
UMLS CUI [2]
C0009402
considered incurable
Descripción

incurable tumor

Tipo de datos

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)
Descripción

disease progression under chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0242656
UMLS CUI [1,2]
C0392920
18 and over
Descripción

18 and over

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
male or female
Descripción

male or female

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
ECOG 0-2
Descripción

ECOG 0-2

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1512162
more than 3 months
Descripción

more than 3 months

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023671
bilirubin no greater than 3 times upper limit of normal (uln)
Descripción

bilirubin no greater than 3 times upper limit of normal (uln)

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005437
calcium less than 1.2 times uln
Descripción

calcium less than 1.2 times uln

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0201925
not pregnant or nursing
Descripción

pregnant or nursing

Tipo de datos

boolean

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

contraception

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0700589
prior concurrent therapy:
Descripción

prior concurrent therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009429
chemotherapy:
Descripción

chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0392920
concurrent chemotherapy allowed
Descripción

concurrent chemotherapy

Tipo de datos

boolean

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

concurrent clinical trial participation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
at least 60 days since prior shark cartilage
Descripción

prior shark cartilage therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C1883024

Similar models

Eligibility Breast Cancer NCT00026117

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
breast or colorectal primary tumor
Item
breast or colorectal primary tumor sites
boolean
C0678222 (UMLS CUI [1])
C0009402 (UMLS CUI [2])
incurable tumor
Item
considered incurable
boolean
C0175969 (UMLS CUI [1])
disease progression under chemotherapy
Item
breast cancer patients must have disease progression after at least 2 different chemotherapy regimens (may include chemotherapy given as an adjuvant treatment)
boolean
C0242656 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
18 and over
Item
18 and over
boolean
C0001779 (UMLS CUI [1])
male or female
Item
male or female
boolean
C0079399 (UMLS CUI [1])
ECOG 0-2
Item
ECOG 0-2
boolean
C1512162 (UMLS CUI [1])
more than 3 months
Item
more than 3 months
boolean
C0023671 (UMLS CUI [1])
bilirubin no greater than 3 times upper limit of normal (uln)
Item
bilirubin no greater than 3 times upper limit of normal (uln)
boolean
C0005437 (UMLS CUI [1])
calcium less than 1.2 times uln
Item
calcium less than 1.2 times uln
boolean
C0201925 (UMLS CUI [1])
pregnant or nursing
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
contraception
Item
fertile patients must use effective contraception
boolean
C0700589 (UMLS CUI [1])
prior concurrent therapy
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
chemotherapy
Item
chemotherapy:
boolean
C0392920 (UMLS CUI [1])
concurrent chemotherapy
Item
concurrent chemotherapy allowed
boolean
C0392920 (UMLS CUI [1,1])
C0009429 (UMLS CUI [1,2])
concurrent clinical trial participation
Item
no concurrent participation in a cytotoxic chemotherapy clinical trial
boolean
C2348568 (UMLS CUI [1])
prior shark cartilage therapy
Item
at least 60 days since prior shark cartilage
boolean
C1514463 (UMLS CUI [1,1])
C1883024 (UMLS CUI [1,2])

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