ID

14868

Beschreibung

Docetaxel vs. Docetaxel-Gemcitabine in Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00191243

Link

https://clinicaltrials.gov/show/NCT00191243

Stichworte

  1. 02.05.16 02.05.16 -
  2. 26.06.16 26.06.16 -
Hochgeladen am

2. Mai 2016

DOI

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Lizenz

Creative Commons BY-NC 3.0

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Eligibility Breast Cancer NCT00191243

Eligibility Breast Cancer NCT00191243

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically verified diagnosis of breast carcinoma, at first diagnosis
Beschreibung

ID.1

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0019638
UMLS CUI [1,2]
C0678222
restricted previous adjuvant chemotherapy (completed >6 months prior the study)
Beschreibung

ID.2

Datentyp

boolean

Alias
UMLS CUI [1]
C0085533
measurable and/or non-measurable disease
Beschreibung

ID.3

Datentyp

boolean

Alias
UMLS CUI [1]
C1513041
previous radiotherapy is allowed if:terminated at least 10 days prior the sudy therapy, at least one target lesion for evaluation of tumor response has not been irradiated
Beschreibung

ID.4

Datentyp

boolean

Alias
UMLS CUI [1]
C1522449
performance status 0-2 (who, zubrod)
Beschreibung

ID.5

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
adequate bone marrow reserve defined
Beschreibung

ID.6

Datentyp

boolean

Alias
UMLS CUI [1]
C0005956
adequate liver / renal functions defined
Beschreibung

ID.7

Datentyp

boolean

Alias
UMLS CUI [1]
C0023895|C0022658
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
any prior systematic chemotherapy for metastatic breast cancer
Beschreibung

ID.8

Datentyp

boolean

Alias
UMLS CUI [1]
C1514457
expected survival time less than 12 weeks
Beschreibung

ID.9

Datentyp

boolean

Alias
UMLS CUI [1]
C0023671
past or current history of malignant neoplasm other than breast carcinoma
Beschreibung

ID.10

Datentyp

boolean

Alias
UMLS CUI [1]
C0085183
except for cured non-melanoma skin cancer or curatively treated in situ carcinoma of the cervix uteri
Beschreibung

ID.11

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1880198
UMLS CUI [1,2]
C0037286|C0851140
known brain metastases/leptomeningeal involvement
Beschreibung

ID.12

Datentyp

boolean

Alias
UMLS CUI [1]
C0220650
active uncontrolled infection
Beschreibung

ID.13

Datentyp

boolean

Alias
UMLS CUI [1]
C3714514
symptomatic peripheral neuropathy > grade 2 according to nci
Beschreibung

ID.14

Datentyp

boolean

Alias
UMLS CUI [1]
C0031117
patients whose lesions are assessable only by radionuclide scan or patients with sclerotic bone lesions as the only site of disease
Beschreibung

ID.15

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0032743|C0748541
UMLS CUI [1,2]
C0748541
concomitant illness that is contraindication to the use of corticosteroids
Beschreibung

ID.16

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0038317
other concomitant serious illness or medical condition, which may worsen due to the treatment
Beschreibung

ID.17

Datentyp

boolean

Alias
UMLS CUI [1]
C0009488

Ähnliche Modelle

Eligibility Breast Cancer NCT00191243

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
histologically verified diagnosis of breast carcinoma, at first diagnosis
boolean
C0019638 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
ID.2
Item
restricted previous adjuvant chemotherapy (completed >6 months prior the study)
boolean
C0085533 (UMLS CUI [1])
ID.3
Item
measurable and/or non-measurable disease
boolean
C1513041 (UMLS CUI [1])
ID.4
Item
previous radiotherapy is allowed if:terminated at least 10 days prior the sudy therapy, at least one target lesion for evaluation of tumor response has not been irradiated
boolean
C1522449 (UMLS CUI [1])
ID.5
Item
performance status 0-2 (who, zubrod)
boolean
C1520224 (UMLS CUI [1])
ID.6
Item
adequate bone marrow reserve defined
boolean
C0005956 (UMLS CUI [1])
ID.7
Item
adequate liver / renal functions defined
boolean
C0023895|C0022658 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.8
Item
any prior systematic chemotherapy for metastatic breast cancer
boolean
C1514457 (UMLS CUI [1])
ID.9
Item
expected survival time less than 12 weeks
boolean
C0023671 (UMLS CUI [1])
ID.10
Item
past or current history of malignant neoplasm other than breast carcinoma
boolean
C0085183 (UMLS CUI [1])
ID.11
Item
except for cured non-melanoma skin cancer or curatively treated in situ carcinoma of the cervix uteri
boolean
C1880198 (UMLS CUI [1,1])
C0037286|C0851140 (UMLS CUI [1,2])
ID.12
Item
known brain metastases/leptomeningeal involvement
boolean
C0220650 (UMLS CUI [1])
ID.13
Item
active uncontrolled infection
boolean
C3714514 (UMLS CUI [1])
ID.14
Item
symptomatic peripheral neuropathy > grade 2 according to nci
boolean
C0031117 (UMLS CUI [1])
ID.15
Item
patients whose lesions are assessable only by radionuclide scan or patients with sclerotic bone lesions as the only site of disease
boolean
C0032743|C0748541 (UMLS CUI [1,1])
C0748541 (UMLS CUI [1,2])
ID.16
Item
concomitant illness that is contraindication to the use of corticosteroids
boolean
C1301624 (UMLS CUI [1,1])
C0038317 (UMLS CUI [1,2])
ID.17
Item
other concomitant serious illness or medical condition, which may worsen due to the treatment
boolean
C0009488 (UMLS CUI [1])

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