ID

16501

Beschreibung

XELOX III. Xeloda in Combination With Eloxatin for Patients With Advanced or Metastatic Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00212615

Link

https://clinicaltrials.gov/show/NCT00212615

Stichworte

  1. 20.07.16 20.07.16 -
Hochgeladen am

20. Juli 2016

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility C04.588.274.476.411.307 NCT00212615

Eligibility C04.588.274.476.411.307 NCT00212615

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
histological proven adenocarcinoma of the colon or rectum
Beschreibung

Adenocarcinoma of colon | Adenocarcinoma of rectum

Datentyp

boolean

Alias
UMLS CUI [1]
C0338106
UMLS CUI [2]
C0149978
measurable or non-measurable disease
Beschreibung

Measurable Disease

Datentyp

boolean

Alias
UMLS CUI [1]
C1513041
performance status 0-2
Beschreibung

performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1518965
adequate renal and hepatic functions
Beschreibung

Renal function | Liver function

Datentyp

boolean

Alias
UMLS CUI [1]
C0232804
UMLS CUI [2]
C0232741
adjuvant chemotherapy must have ended 180 days before inclusion
Beschreibung

Adjuvant Chemotherapy Ended

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0085533
UMLS CUI [1,2]
C1272693
written informed consent prior to randomization
Beschreibung

Informed consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior treatment with eloxatin or xeloda
Beschreibung

Eloxatin | Xeloda

Datentyp

boolean

Alias
UMLS CUI [1]
C1135117
UMLS CUI [2]
C0724419
peripheral neuropathy
Beschreibung

Peripheral Neuropathy

Datentyp

boolean

Alias
UMLS CUI [1]
C0031117
evidence of cns metastasis
Beschreibung

CNS metastases Evidence of

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0686377
UMLS CUI [1,2]
C0332120
other serious illness or medical conditions (including contraindication to 5 fu e.g.: angor, myocardial infarction within 6 months)
Beschreibung

Illness Serious | Other medical condition | Medical contraindication Fluorouracil | Angina Pectoris | Myocardial Infarction

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0205404
UMLS CUI [2]
C3843040
UMLS CUI [3,1]
C1301624
UMLS CUI [3,2]
C0016360
UMLS CUI [4]
C0002962
UMLS CUI [5]
C0027051
past history of malignant neoplasm within the past five years, except curatively treated non melanoma skin cancer
Beschreibung

Malignant Neoplasms | Skin carcinoma curative treatment

Datentyp

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2,1]
C0699893
UMLS CUI [2,2]
C1273390
administration of any other experimental drug under investigation within 2 weeks before randomisation
Beschreibung

Investigational New Drugs

Datentyp

boolean

Alias
UMLS CUI [1]
C0013230
pregnant or breast feeding women
Beschreibung

Pregnancy | Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
fertile patients must use adequate contraceptives
Beschreibung

Fertility Contraceptives

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0015895
UMLS CUI [1,2]
C0009871

Ähnliche Modelle

Eligibility C04.588.274.476.411.307 NCT00212615

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Adenocarcinoma of colon | Adenocarcinoma of rectum
Item
histological proven adenocarcinoma of the colon or rectum
boolean
C0338106 (UMLS CUI [1])
C0149978 (UMLS CUI [2])
Measurable Disease
Item
measurable or non-measurable disease
boolean
C1513041 (UMLS CUI [1])
performance status
Item
performance status 0-2
boolean
C1518965 (UMLS CUI [1])
Renal function | Liver function
Item
adequate renal and hepatic functions
boolean
C0232804 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
Adjuvant Chemotherapy Ended
Item
adjuvant chemotherapy must have ended 180 days before inclusion
boolean
C0085533 (UMLS CUI [1,1])
C1272693 (UMLS CUI [1,2])
Informed consent
Item
written informed consent prior to randomization
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Eloxatin | Xeloda
Item
prior treatment with eloxatin or xeloda
boolean
C1135117 (UMLS CUI [1])
C0724419 (UMLS CUI [2])
Peripheral Neuropathy
Item
peripheral neuropathy
boolean
C0031117 (UMLS CUI [1])
CNS metastases Evidence of
Item
evidence of cns metastasis
boolean
C0686377 (UMLS CUI [1,1])
C0332120 (UMLS CUI [1,2])
Illness Serious | Other medical condition | Medical contraindication Fluorouracil | Angina Pectoris | Myocardial Infarction
Item
other serious illness or medical conditions (including contraindication to 5 fu e.g.: angor, myocardial infarction within 6 months)
boolean
C0221423 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C3843040 (UMLS CUI [2])
C1301624 (UMLS CUI [3,1])
C0016360 (UMLS CUI [3,2])
C0002962 (UMLS CUI [4])
C0027051 (UMLS CUI [5])
Malignant Neoplasms | Skin carcinoma curative treatment
Item
past history of malignant neoplasm within the past five years, except curatively treated non melanoma skin cancer
boolean
C0006826 (UMLS CUI [1])
C0699893 (UMLS CUI [2,1])
C1273390 (UMLS CUI [2,2])
Investigational New Drugs
Item
administration of any other experimental drug under investigation within 2 weeks before randomisation
boolean
C0013230 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or breast feeding women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Fertility Contraceptives
Item
fertile patients must use adequate contraceptives
boolean
C0015895 (UMLS CUI [1,1])
C0009871 (UMLS CUI [1,2])

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