ID

79

Beskrivning

ODM derived from http://clinicaltrials.gov/ct2/show/record/NCT00661609

Länk

http://clinicaltrials.gov/ct2/show/record/NCT00661609

Nyckelord

  1. 2011-11-18 2011-11-18 -
  2. 2014-03-26 2014-03-26 - Martin Dugas
  3. 2021-09-17 2021-09-17 -
Uppladdad den

18 november 2011

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC 3.0 Legacy

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility NCT00661609 Bladder Cancer

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion criteria
Beskrivning

Inclusion criteria

Confirmed urothelial cancer (cancer of the bladder, renal pelvis, ureter, or urethra)
Beskrivning

Urothelial cancer

Datatyp

boolean

Tumor, Node, Metastasis (TNM) Stage IV urothelial cancer that can not be helped by curative surgery and/or curative radiotherapy
Beskrivning

Stage IV

Datatyp

boolean

Must have had a maximum of 2 prior chemotherapeutic regimens, one for unremovable and/or metastasized disease, and the other in the adjuvant or neo-adjuvant setting
Beskrivning

Prior chemotherapy

Datatyp

boolean

Ambulatory and capable of all selfcare more than 50% of waking hours
Beskrivning

General status

Datatyp

boolean

Exclusion criteria
Beskrivning

Exclusion criteria

Prior treatment with investigational or standard anti-cancer agents, including radiotherapy, within 4 weeks prior to first dose of study medication, 6 weeks if prior systemic mitomycin, nitrosourea, or suramin.
Beskrivning

Prior treatment

Datatyp

boolean

Inadequate bone marrow reserve
Beskrivning

Bone marrow

Datatyp

boolean

Inadequate liver function in the presence of liver metastases
Beskrivning

Liver

Datatyp

boolean

Impaired renal function
Beskrivning

Kidney

Datatyp

boolean

Medical concepts
Beskrivning

Medical concepts

Diagnosis
Beskrivning

Diagnosis

Datatyp

string

Alias
UMLS CUI
C0011900
SNOMED CT 2010_0731
439401001
LOINC Version 232
MTHU008876
Carcinoma of bladder
Beskrivning

Bladder Cancer

Datatyp

string

Alias
UMLS CUI
C0699885
SNOMED CT 2010_0731
255108000
MedDRA 13.1
10005014
Diagnostic Neoplasm Staging
Beskrivning

Tumor Staging

Datatyp

string

Alias
UMLS CUI
C0027646
SNOMED CT 2010_0731
254292007
LOINC Version 232
LP78422-0
Chemotherapy
Beskrivning

Chemotherapy

Datatyp

string

Alias
UMLS CUI
C0392920
SNOMED CT 2010_0731
150415003
Ambulatory
Beskrivning

Ambulatory

Datatyp

string

Alias
UMLS CUI
C0439841
Radiotherapy
Beskrivning

Radiotherapy

Datatyp

string

Alias
UMLS CUI
C1522449
SNOMED CT 2010_0731
302505005
White Blood Cells
Beskrivning

WBC

Datatyp

string

Alias
SNOMED CT 2010_0731
767002
LOINC Version 232
6690-2
Platelet count - finding
Beskrivning

Platelet count

Datatyp

string

Alias
UMLS CUI
C1287267
SNOMED CT 2010_0731
365632008
LOINC Version 232
777-3
Hemoglobin
Beskrivning

Hemoglobin

Datatyp

string

Alias
UMLS CUI
C0019046
SNOMED CT 2010_0731
38082009
MedDRA 13.1
10019481
LOINC Version 232
LP14449-0
Metastatic Malignant Neoplasm to the Liver
Beskrivning

Liver Metastasis

Datatyp

string

Alias
UMLS CUI
C0494165
SNOMED CT 2010_0731
94381002
MedDRA 13.1
10027457
ICD-10-CM Version 2010
C78.7
ICD-9-CM Version 2011
197.7

Similar models

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion criteria
Urothelial cancer
Item
Confirmed urothelial cancer (cancer of the bladder, renal pelvis, ureter, or urethra)
boolean
Stage IV
Item
Tumor, Node, Metastasis (TNM) Stage IV urothelial cancer that can not be helped by curative surgery and/or curative radiotherapy
boolean
Prior chemotherapy
Item
Must have had a maximum of 2 prior chemotherapeutic regimens, one for unremovable and/or metastasized disease, and the other in the adjuvant or neo-adjuvant setting
boolean
General status
Item
Ambulatory and capable of all selfcare more than 50% of waking hours
boolean
Item Group
Exclusion criteria
Prior treatment
Item
Prior treatment with investigational or standard anti-cancer agents, including radiotherapy, within 4 weeks prior to first dose of study medication, 6 weeks if prior systemic mitomycin, nitrosourea, or suramin.
boolean
Bone marrow
Item
Inadequate bone marrow reserve
boolean
Liver
Item
Inadequate liver function in the presence of liver metastases
boolean
Kidney
Item
Impaired renal function
boolean
Item Group
Medical concepts
Diagnosis
Item
Diagnosis
string
C0011900 (UMLS CUI)
439401001 (SNOMED CT 2010_0731)
MTHU008876 (LOINC Version 232)
Bladder Cancer
Item
Carcinoma of bladder
string
C0699885 (UMLS CUI)
255108000 (SNOMED CT 2010_0731)
10005014 (MedDRA 13.1)
Tumor Staging
Item
Diagnostic Neoplasm Staging
string
C0027646 (UMLS CUI)
254292007 (SNOMED CT 2010_0731)
LP78422-0 (LOINC Version 232)
Chemotherapy
Item
Chemotherapy
string
C0392920 (UMLS CUI)
150415003 (SNOMED CT 2010_0731)
Ambulatory
Item
Ambulatory
string
C0439841 (UMLS CUI)
Radiotherapy
Item
Radiotherapy
string
C1522449 (UMLS CUI)
302505005 (SNOMED CT 2010_0731)
WBC
Item
White Blood Cells
string
767002 (SNOMED CT 2010_0731)
6690-2 (LOINC Version 232)
Platelet count
Item
Platelet count - finding
string
C1287267 (UMLS CUI)
365632008 (SNOMED CT 2010_0731)
777-3 (LOINC Version 232)
Hemoglobin
Item
Hemoglobin
string
C0019046 (UMLS CUI)
38082009 (SNOMED CT 2010_0731)
10019481 (MedDRA 13.1)
LP14449-0 (LOINC Version 232)
Liver Metastasis
Item
Metastatic Malignant Neoplasm to the Liver
string
C0494165 (UMLS CUI)
94381002 (SNOMED CT 2010_0731)
10027457 (MedDRA 13.1)
C78.7 (ICD-10-CM Version 2010)
197.7 (ICD-9-CM Version 2011)

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

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