ID

22114

Description

Survival Study of Docetaxel and Carboplatin as Neo-Adjuvant Vs Adjuvant Chemotherapy in Early Stage NSLC; ODM derived from: https://clinicaltrials.gov/show/NCT00321334

Link

https://clinicaltrials.gov/show/NCT00321334

Keywords

Versions (1)
  1. 5/20/17 5/20/17 -
Uploaded on

May 20, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Non-small Cell Lung Cancer NCT00321334

English

Eligibility Non-small Cell Lung Cancer NCT00321334

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically or cytologically confirmed stage ib-iiia non-small cell lung cancer patients,without previous chemotherapy, radiotherapy or target-therapy;
Description

Non-Small Cell Lung Carcinoma TNM clinical staging | Chemotherapy Absent | Therapeutic radiology procedure Absent | Targeted Therapy Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C3258246
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C1522449
UMLS CUI [3,2]
C0332197
UMLS CUI [4,1]
C2985566
UMLS CUI [4,2]
C0332197
age from 18 to 75;
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
ps with ecoc 0-1;
Description

ECOG performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
adequate haematological and hepatic- renal function;
Description

Hematologic function | Liver function | Renal function

Data type

boolean

Alias
UMLS CUI [1]
C0221130
UMLS CUI [2]
C0232741
UMLS CUI [3]
C0232804
expected to live longer than 12 months;
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
the informed consent should be signed.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with small cell lung cancer;
Description

Small cell carcinoma of lung

Data type

boolean

Alias
UMLS CUI [1]
C0149925
already receiving any prior anti-cancer treatment;
Description

cancer treatment

Data type

boolean

Alias
UMLS CUI [1]
C0920425
pregnant women;
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
uncontrolled diabetes, mental disease;
Description

Diabetic - poor control | Mental disorder

Data type

boolean

Alias
UMLS CUI [1]
C0421258
UMLS CUI [2]
C0004936
hepatic and renal function failure;
Description

Liver Failure | Kidney Failure

Data type

boolean

Alias
UMLS CUI [1]
C0085605
UMLS CUI [2]
C0035078
the investigators believe the patient is not suitable to be enrolled in the study
Description

Study Subject Participation Status Inappropriate

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548788
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Similar models

Eligibility Non-small Cell Lung Cancer NCT00321334

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma TNM clinical staging | Chemotherapy Absent | Therapeutic radiology procedure Absent | Targeted Therapy Absent
Item
histologically or cytologically confirmed stage ib-iiia non-small cell lung cancer patients,without previous chemotherapy, radiotherapy or target-therapy;
boolean
C0007131 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C1522449 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C2985566 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
Age
Item
age from 18 to 75;
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
ps with ecoc 0-1;
boolean
C1520224 (UMLS CUI [1])
Hematologic function | Liver function | Renal function
Item
adequate haematological and hepatic- renal function;
boolean
C0221130 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Life Expectancy
Item
expected to live longer than 12 months;
boolean
C0023671 (UMLS CUI [1])
Informed Consent
Item
the informed consent should be signed.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Small cell carcinoma of lung
Item
patients with small cell lung cancer;
boolean
C0149925 (UMLS CUI [1])
cancer treatment
Item
already receiving any prior anti-cancer treatment;
boolean
C0920425 (UMLS CUI [1])
Pregnancy
Item
pregnant women;
boolean
C0032961 (UMLS CUI [1])
Diabetic - poor control | Mental disorder
Item
uncontrolled diabetes, mental disease;
boolean
C0421258 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
Liver Failure | Kidney Failure
Item
hepatic and renal function failure;
boolean
C0085605 (UMLS CUI [1])
C0035078 (UMLS CUI [2])
Study Subject Participation Status Inappropriate
Item
the investigators believe the patient is not suitable to be enrolled in the study
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
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