ID

16015

Description

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

Lien

https://clinicaltrials.gov/show/NCT00026117

Mots-clés

  1. 01/05/2016 01/05/2016 -
  2. 26/06/2016 26/06/2016 -
  3. 26/06/2016 26/06/2016 -
Téléchargé le

26 juin 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Breast Cancer NCT00026117

Eligibility Breast Cancer NCT00026117

Criteria
Description

Criteria

breast or colorectal primary tumor sites
Description

breast or colorectal primary tumor

Type de données

boolean

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

incurable tumor

Type de données

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

disease progression under chemotherapy

Type de données

boolean

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

18 and over

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
male or female
Description

male or female

Type de données

boolean

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

ECOG 0-2

Type de données

boolean

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

more than 3 months

Type de données

boolean

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

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

Type de données

boolean

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

calcium less than 1.2 times uln

Type de données

boolean

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

pregnant or nursing

Type de données

boolean

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

contraception

Type de données

boolean

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

prior concurrent therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0009429
chemotherapy:
Description

chemotherapy

Type de données

boolean

Alias
UMLS CUI [1]
C0392920
concurrent chemotherapy allowed
Description

concurrent chemotherapy

Type de données

boolean

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

concurrent clinical trial participation

Type de données

boolean

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

prior shark cartilage therapy

Type de données

boolean

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

Similar models

Eligibility Breast Cancer NCT00026117

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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