ID

31054

Beskrivning

Zactima in Non Small Cell Lung Cancer (NSCLC) ELderly Patients In Combination With or Versus Gemcitabine; ODM derived from: https://clinicaltrials.gov/show/NCT00753714

Länk

https://clinicaltrials.gov/show/NCT00753714

Nyckelord

Versioner (1)
  1. 2018-07-15 2018-07-15 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

15 juli 2018

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0
Modellkommentarer :

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

Tillbaka till modellkommentarer
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 Non Small Cell Lung Cancer NCT00753714

Engelsk

Eligibility Non Small Cell Lung Cancer NCT00753714

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologic or cytologic confirmation of advanced nsclc (stage iiib with supraclavicular lymph node metastases or pleural effusion or stage iv) on entry into study
Beskrivning

Non-Small Cell Lung Carcinoma Advanced TNM clinical staging | Secondary malignant neoplasm of lymph node Supraclavicular | Pleural effusion | Non-Small Cell Lung Carcinoma TNM clinical staging

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C0205179
UMLS CUI [1,3]
C3258246
UMLS CUI [2,1]
C0686619
UMLS CUI [2,2]
C1550301
UMLS CUI [3]
C0032227
UMLS CUI [4,1]
C0007131
UMLS CUI [4,2]
C3258246
one or more measurable lesions at least 10 mm in the longest diameter (ld) by spiral ct scan or 20 mm with conventional techniques according to recist criteria
Beskrivning

Measurable lesion Quantity | Longest Diameter Spiral CT scan | Longest Diameter Technique conventional

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C1265611
UMLS CUI [2,1]
C0552406
UMLS CUI [2,2]
C0860888
UMLS CUI [3,1]
C0552406
UMLS CUI [3,2]
C0449851
UMLS CUI [3,3]
C0439858
chemotherapy-naïve (prior chemotherapy in the adjuvant setting completed more than 3 months before the trial entry is accepted).
Beskrivning

Chemotherapy naive | Adjuvant Chemotherapy Previous Completed

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0919936
UMLS CUI [2,1]
C0085533
UMLS CUI [2,2]
C0205156
UMLS CUI [2,3]
C0205197
female or male aged 70 years or above
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients must not have received prior anti-cancer therapy except in the adjuvant setting
Beskrivning

Cancer treatment Previous | Exception Adjuvant therapy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C0205156
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0677850
inadequate end-organ function or evidence of severe or uncontrolled systemic disease or any concurrent condition which in the investigator's opinion makes it undesirable for the patient to participate in the trial
Beskrivning

Organ function Inadequate | Systemic disease Severe | Systemic disease Uncontrolled | Condition Study Subject Participation Status Unfavorable

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0678852
UMLS CUI [1,2]
C0205412
UMLS CUI [2,1]
C0442893
UMLS CUI [2,2]
C0205082
UMLS CUI [3,1]
C0442893
UMLS CUI [3,2]
C0205318
UMLS CUI [4,1]
C0348080
UMLS CUI [4,2]
C2348568
UMLS CUI [4,3]
C3640815
significant cardiovascular event (e.g. myocardial infarction, superior vena cava [svc] syndrome, new york heart association [nyha] classification of heart disease ³2) within 3 months before entry, or presence of cardiac disease that in the opinion of
Beskrivning

Cardiovascular event | Myocardial Infarction | Superior Vena Cava Syndrome | Heart Disease New York Heart Association Classification

Datatyp

boolean

Alias
UMLS CUI [1]
C1320716
UMLS CUI [2]
C0027051
UMLS CUI [3]
C0038833
UMLS CUI [4,1]
C0018799
UMLS CUI [4,2]
C1275491
history of arrhythmia or qtc with bazett's correction unmeasurable or ≥ 480 msec on screening ecg
Beskrivning

Cardiac Arrhythmia | QTc Bazett formula Measurement Unsuccessful | ECG QTc interval Bazett formula

Datatyp

boolean

Alias
UMLS CUI [1]
C0003811
UMLS CUI [2,1]
C0860814
UMLS CUI [2,2]
C4038411
UMLS CUI [2,3]
C0242485
UMLS CUI [2,4]
C1272705
UMLS CUI [3,1]
C2216079
UMLS CUI [3,2]
C4038411
Tillbaka till toppen

Similar models

Eligibility Non Small Cell Lung Cancer NCT00753714

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma Advanced TNM clinical staging | Secondary malignant neoplasm of lymph node Supraclavicular | Pleural effusion | Non-Small Cell Lung Carcinoma TNM clinical staging
Item
histologic or cytologic confirmation of advanced nsclc (stage iiib with supraclavicular lymph node metastases or pleural effusion or stage iv) on entry into study
boolean
C0007131 (UMLS CUI [1,1])
C0205179 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0686619 (UMLS CUI [2,1])
C1550301 (UMLS CUI [2,2])
C0032227 (UMLS CUI [3])
C0007131 (UMLS CUI [4,1])
C3258246 (UMLS CUI [4,2])
Measurable lesion Quantity | Longest Diameter Spiral CT scan | Longest Diameter Technique conventional
Item
one or more measurable lesions at least 10 mm in the longest diameter (ld) by spiral ct scan or 20 mm with conventional techniques according to recist criteria
boolean
C1513041 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0552406 (UMLS CUI [2,1])
C0860888 (UMLS CUI [2,2])
C0552406 (UMLS CUI [3,1])
C0449851 (UMLS CUI [3,2])
C0439858 (UMLS CUI [3,3])
Chemotherapy naive | Adjuvant Chemotherapy Previous Completed
Item
chemotherapy-naïve (prior chemotherapy in the adjuvant setting completed more than 3 months before the trial entry is accepted).
boolean
C0392920 (UMLS CUI [1,1])
C0919936 (UMLS CUI [1,2])
C0085533 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
C0205197 (UMLS CUI [2,3])
Age
Item
female or male aged 70 years or above
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Cancer treatment Previous | Exception Adjuvant therapy
Item
patients must not have received prior anti-cancer therapy except in the adjuvant setting
boolean
C0920425 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0677850 (UMLS CUI [2,2])
Organ function Inadequate | Systemic disease Severe | Systemic disease Uncontrolled | Condition Study Subject Participation Status Unfavorable
Item
inadequate end-organ function or evidence of severe or uncontrolled systemic disease or any concurrent condition which in the investigator's opinion makes it undesirable for the patient to participate in the trial
boolean
C0678852 (UMLS CUI [1,1])
C0205412 (UMLS CUI [1,2])
C0442893 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0442893 (UMLS CUI [3,1])
C0205318 (UMLS CUI [3,2])
C0348080 (UMLS CUI [4,1])
C2348568 (UMLS CUI [4,2])
C3640815 (UMLS CUI [4,3])
Cardiovascular event | Myocardial Infarction | Superior Vena Cava Syndrome | Heart Disease New York Heart Association Classification
Item
significant cardiovascular event (e.g. myocardial infarction, superior vena cava [svc] syndrome, new york heart association [nyha] classification of heart disease ³2) within 3 months before entry, or presence of cardiac disease that in the opinion of
boolean
C1320716 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
C0038833 (UMLS CUI [3])
C0018799 (UMLS CUI [4,1])
C1275491 (UMLS CUI [4,2])
Cardiac Arrhythmia | QTc Bazett formula Measurement Unsuccessful | ECG QTc interval Bazett formula
Item
history of arrhythmia or qtc with bazett's correction unmeasurable or ≥ 480 msec on screening ecg
boolean
C0003811 (UMLS CUI [1])
C0860814 (UMLS CUI [2,1])
C4038411 (UMLS CUI [2,2])
C0242485 (UMLS CUI [2,3])
C1272705 (UMLS CUI [2,4])
C2216079 (UMLS CUI [3,1])
C4038411 (UMLS CUI [3,2])
Tillbaka till toppen 

Kontakt

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

Fält markerade med * är obligatoriska.

Hjälp

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