ID

16015

Beschrijving

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

Trefwoorden

  1. 01-05-16 01-05-16 -
  2. 26-06-16 26-06-16 -
  3. 26-06-16 26-06-16 -
Geüploaded op

26 juni 2016

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Breast Cancer NCT00026117

Eligibility Breast Cancer NCT00026117

Criteria
Beschrijving

Criteria

breast or colorectal primary tumor sites
Beschrijving

breast or colorectal primary tumor

Datatype

boolean

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

incurable tumor

Datatype

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)
Beschrijving

disease progression under chemotherapy

Datatype

boolean

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

18 and over

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
male or female
Beschrijving

male or female

Datatype

boolean

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

ECOG 0-2

Datatype

boolean

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

more than 3 months

Datatype

boolean

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

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

Datatype

boolean

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

calcium less than 1.2 times uln

Datatype

boolean

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

pregnant or nursing

Datatype

boolean

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

contraception

Datatype

boolean

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

prior concurrent therapy

Datatype

boolean

Alias
UMLS CUI [1]
C0009429
chemotherapy:
Beschrijving

chemotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C0392920
concurrent chemotherapy allowed
Beschrijving

concurrent chemotherapy

Datatype

boolean

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

concurrent clinical trial participation

Datatype

boolean

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

prior shark cartilage therapy

Datatype

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)
Datatype
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])

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial