ID

22138

Description

Alimta and Gemcitabine in Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00434135

Link

https://clinicaltrials.gov/show/NCT00434135

Keywords

Versions (1)
  1. 5/21/17 5/21/17 -
Uploaded on

May 21, 2017

DOI

To request one please log in.

License

Creative Commons BY 4.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Non-Small Cell Lung Cancer NCT00434135

English

Eligibility Non-Small Cell Lung Cancer NCT00434135

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. patients with histologically or cytologically confirmed locally advanced (stage iiib) or metastatic (stage iv) nsclc
Description

Non-Small Cell Lung Carcinoma Advanced Local TNM clinical staging | Non-small cell lung cancer metastatic TNM clinical staging

Data type

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C0205179
UMLS CUI [1,3]
C0205276
UMLS CUI [1,4]
C3258246
UMLS CUI [2,1]
C0278987
UMLS CUI [2,2]
C3258246
2. no previous adjuvant or palliative chemotherapy
Description

Adjuvant Chemotherapy Absent | Chemotherapy Palliative Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0085533
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C1285530
UMLS CUI [2,3]
C0332197
3. no previous radiotherapy
Description

Therapeutic radiology procedure Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0332197
4. presence of at least one unidimensionally measurable lesion (appendix 2)
Description

Measurable lesion Linear Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C0205132
UMLS CUI [1,3]
C1265611
5. ecog performance status of 0 or 1 (appendix 3)
Description

ECOG performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
6. charlson score ≤ 2 (appendix 4)
Description

Charlson Comorbidity Index

Data type

boolean

Alias
UMLS CUI [1]
C3714916
7. adequate bone marrow function (absolute neutrophil count ≥ 2 x 109/l, platelet count
Description

Bone Marrow function | Absolute neutrophil count | Platelet Count measurement

Data type

boolean

Alias
UMLS CUI [1,1]
C0005953
UMLS CUI [1,2]
C0031843
UMLS CUI [2]
C0948762
UMLS CUI [3]
C0032181
≥ 100 x 109/l, and hemoglobin level ≥ 100 g/l), and adequate liver function (bilirubin level < two times the upper limit of normal, ast and/or alt < three times the upper limit of normal, prothrombin time < 1.5 times control), and creatinine clearance ≥ 60 ml/min.
Description

Hemoglobin measurement | Liver function | Serum total bilirubin measurement | Aspartate aminotransferase measurement | Alanine aminotransferase measurement | Prothrombin time | Creatinine clearance measurement

Data type

boolean

Alias
UMLS CUI [1]
C0518015
UMLS CUI [2]
C0232741
UMLS CUI [3]
C1278039
UMLS CUI [4]
C0201899
UMLS CUI [5]
C0201836
UMLS CUI [6]
C1533047
UMLS CUI [7]
C0373595
8. absence of symptomatic cns metastases (patients with cerebral metastases treated with brain irradiation may be included), severe cardiac arrhythmia or heart failure, second or third degree heart block or acute myocardial infarction within 4 months prior to study entry.
Description

CNS metastases Symptomatic Absent | Irradiation of whole brain Cerebral metastasis | Cardiac Arrhythmia Severe | Heart failure Severe | Second degree atrioventricular block | Complete atrioventricular block | Myocardial Infarction

Data type

boolean

Alias
UMLS CUI [1,1]
C0686377
UMLS CUI [1,2]
C0231220
UMLS CUI [1,3]
C0332197
UMLS CUI [2,1]
C2064932
UMLS CUI [2,2]
C0555278
UMLS CUI [3,1]
C0003811
UMLS CUI [3,2]
C0205082
UMLS CUI [4,1]
C0018801
UMLS CUI [4,2]
C0205082
UMLS CUI [5]
C0264906
UMLS CUI [6]
C0151517
UMLS CUI [7]
C0027051
9. no major surgery or pleurodesis within 14 days prior to enrollment.
Description

Major surgery Absent | Pleurodesis Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0679637
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0189557
UMLS CUI [2,2]
C0332197
10. life expectancy of at least 12 weeks.
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
11. no previous or concurrent malignancy, except inactive non-melanoma skin cancer, in situ carcinoma of the cervix, or other cancer if the patient has been disease-free for more than 5 years.
Description

Malignant Neoplasms Absent | Skin carcinoma inactive | Carcinoma in situ of uterine cervix inactive | Malignant Neoplasm Disease Free of

Data type

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0699893
UMLS CUI [2,2]
C0544452
UMLS CUI [3,1]
C0851140
UMLS CUI [3,2]
C0544452
UMLS CUI [4,1]
C0006826
UMLS CUI [4,2]
C0012634
UMLS CUI [4,3]
C0332296
12. written informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. any unstable systemic disease (including active infection, uncontrolled hypertension, unstable angina, congestive heart failure, serious cardiac arrhythmia requiring medication, hepatic, renal or metabolic disease).
Description

Systemic disease Unstable | Communicable Disease | Uncontrolled hypertension | Angina, Unstable | Congestive heart failure | Cardiac Arrhythmia Serious Requirement Pharmaceutical Preparations | Liver disease | Kidney Disease | Metabolic Diseases

Data type

boolean

Alias
UMLS CUI [1,1]
C0442893
UMLS CUI [1,2]
C0443343
UMLS CUI [2]
C0009450
UMLS CUI [3]
C1868885
UMLS CUI [4]
C0002965
UMLS CUI [5]
C0018802
UMLS CUI [6,1]
C0003811
UMLS CUI [6,2]
C0205404
UMLS CUI [6,3]
C1514873
UMLS CUI [6,4]
C0013227
UMLS CUI [7]
C0023895
UMLS CUI [8]
C0022658
UMLS CUI [9]
C0025517
2. patients with clinically significant effusions.
Description

Effusion Clinical Significance

Data type

boolean

Alias
UMLS CUI [1,1]
C0013687
UMLS CUI [1,2]
C2826293
3. any other malignancies within 5 years that could affect therapy evaluation
Description

Malignant Neoplasms Affecting Therapy Evaluation

Data type

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C1515410
Back to the top of the page

Similar models

Eligibility Non-Small Cell Lung Cancer NCT00434135

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma Advanced Local TNM clinical staging | Non-small cell lung cancer metastatic TNM clinical staging
Item
1. patients with histologically or cytologically confirmed locally advanced (stage iiib) or metastatic (stage iv) nsclc
boolean
C0007131 (UMLS CUI [1,1])
C0205179 (UMLS CUI [1,2])
C0205276 (UMLS CUI [1,3])
C3258246 (UMLS CUI [1,4])
C0278987 (UMLS CUI [2,1])
C3258246 (UMLS CUI [2,2])
Adjuvant Chemotherapy Absent | Chemotherapy Palliative Absent
Item
2. no previous adjuvant or palliative chemotherapy
boolean
C0085533 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C1285530 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Therapeutic radiology procedure Absent
Item
3. no previous radiotherapy
boolean
C1522449 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Measurable lesion Linear Quantity
Item
4. presence of at least one unidimensionally measurable lesion (appendix 2)
boolean
C1513041 (UMLS CUI [1,1])
C0205132 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
ECOG performance status
Item
5. ecog performance status of 0 or 1 (appendix 3)
boolean
C1520224 (UMLS CUI [1])
Charlson Comorbidity Index
Item
6. charlson score ≤ 2 (appendix 4)
boolean
C3714916 (UMLS CUI [1])
Bone Marrow function | Absolute neutrophil count | Platelet Count measurement
Item
7. adequate bone marrow function (absolute neutrophil count ≥ 2 x 109/l, platelet count
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0948762 (UMLS CUI [2])
C0032181 (UMLS CUI [3])
Hemoglobin measurement | Liver function | Serum total bilirubin measurement | Aspartate aminotransferase measurement | Alanine aminotransferase measurement | Prothrombin time | Creatinine clearance measurement
Item
≥ 100 x 109/l, and hemoglobin level ≥ 100 g/l), and adequate liver function (bilirubin level < two times the upper limit of normal, ast and/or alt < three times the upper limit of normal, prothrombin time < 1.5 times control), and creatinine clearance ≥ 60 ml/min.
boolean
C0518015 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C1278039 (UMLS CUI [3])
C0201899 (UMLS CUI [4])
C0201836 (UMLS CUI [5])
C1533047 (UMLS CUI [6])
C0373595 (UMLS CUI [7])
CNS metastases Symptomatic Absent | Irradiation of whole brain Cerebral metastasis | Cardiac Arrhythmia Severe | Heart failure Severe | Second degree atrioventricular block | Complete atrioventricular block | Myocardial Infarction
Item
8. absence of symptomatic cns metastases (patients with cerebral metastases treated with brain irradiation may be included), severe cardiac arrhythmia or heart failure, second or third degree heart block or acute myocardial infarction within 4 months prior to study entry.
boolean
C0686377 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C2064932 (UMLS CUI [2,1])
C0555278 (UMLS CUI [2,2])
C0003811 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0018801 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0264906 (UMLS CUI [5])
C0151517 (UMLS CUI [6])
C0027051 (UMLS CUI [7])
Major surgery Absent | Pleurodesis Absent
Item
9. no major surgery or pleurodesis within 14 days prior to enrollment.
boolean
C0679637 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0189557 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Life Expectancy
Item
10. life expectancy of at least 12 weeks.
boolean
C0023671 (UMLS CUI [1])
Malignant Neoplasms Absent | Skin carcinoma inactive | Carcinoma in situ of uterine cervix inactive | Malignant Neoplasm Disease Free of
Item
11. no previous or concurrent malignancy, except inactive non-melanoma skin cancer, in situ carcinoma of the cervix, or other cancer if the patient has been disease-free for more than 5 years.
boolean
C0006826 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0699893 (UMLS CUI [2,1])
C0544452 (UMLS CUI [2,2])
C0851140 (UMLS CUI [3,1])
C0544452 (UMLS CUI [3,2])
C0006826 (UMLS CUI [4,1])
C0012634 (UMLS CUI [4,2])
C0332296 (UMLS CUI [4,3])
Informed Consent
Item
12. written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Systemic disease Unstable | Communicable Disease | Uncontrolled hypertension | Angina, Unstable | Congestive heart failure | Cardiac Arrhythmia Serious Requirement Pharmaceutical Preparations | Liver disease | Kidney Disease | Metabolic Diseases
Item
1. any unstable systemic disease (including active infection, uncontrolled hypertension, unstable angina, congestive heart failure, serious cardiac arrhythmia requiring medication, hepatic, renal or metabolic disease).
boolean
C0442893 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0009450 (UMLS CUI [2])
C1868885 (UMLS CUI [3])
C0002965 (UMLS CUI [4])
C0018802 (UMLS CUI [5])
C0003811 (UMLS CUI [6,1])
C0205404 (UMLS CUI [6,2])
C1514873 (UMLS CUI [6,3])
C0013227 (UMLS CUI [6,4])
C0023895 (UMLS CUI [7])
C0022658 (UMLS CUI [8])
C0025517 (UMLS CUI [9])
Effusion Clinical Significance
Item
2. patients with clinically significant effusions.
boolean
C0013687 (UMLS CUI [1,1])
C2826293 (UMLS CUI [1,2])
Malignant Neoplasms Affecting Therapy Evaluation
Item
3. any other malignancies within 5 years that could affect therapy evaluation
boolean
C0006826 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C1515410 (UMLS CUI [1,3])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

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