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Eligibility Carcinoma, Non-Small Cell Lung NCT00973310

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 18-70 years，
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patients with stage iiia-iiib nsclc
Description

Non-Small Cell Lung Carcinoma TNM clinical staging

Data type

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C3258246
adequate hematologic (wbc and platelet counts within normal limits), hepatic (total bilirubin level <= two times the upper limit of normal), and renal (creatinine clearance >= 50ml/min) functions
Description

Hematologic function | White Blood Cell Count procedure | Platelet Count measurement | Liver function | Serum total bilirubin measurement | Renal function | Creatinine clearance measurement

Data type

boolean

Alias
UMLS CUI [1]
C0221130
UMLS CUI [2]
C0023508
UMLS CUI [3]
C0032181
UMLS CUI [4]
C0232741
UMLS CUI [5]
C1278039
UMLS CUI [6]
C0232804
UMLS CUI [7]
C0373595
no history of chemotherapy or less than 4 cycles neoadjuvant chemotherapy
Description

Chemotherapy Absent | Chemotherapy cycle Neoadjuvant Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C1302181
UMLS CUI [2,2]
C0600558
UMLS CUI [2,3]
C1265611
can not tolerate or refuse concurrent chemoradiotherapy
Description

Intolerance Chemoradiotherapy | Chemoradiotherapy Refused

Data type

boolean

Alias
UMLS CUI [1,1]
C0231199
UMLS CUI [1,2]
C0436307
UMLS CUI [2,1]
C0436307
UMLS CUI [2,2]
C1705116
no history of thoracic rt
Description

Radiotherapy to thorax Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C4038705
UMLS CUI [1,2]
C0332197
written informed consent obtained
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
with other malignancy
Description

Cancer Other

Data type

boolean

Alias
UMLS CUI [1]
C1707251
with severe cardiopulmonary disease
Description

Cardiopulmonary disease Severe

Data type

boolean

Alias
UMLS CUI [1,1]
C0034072
UMLS CUI [1,2]
C0205082
compromised liver or renal function that could not tolerate the combined therapy
Description

Liver Dysfunction | Renal function | Intolerance Combined Modality Therapy

Data type

boolean

Alias
UMLS CUI [1]
C0086565
UMLS CUI [2]
C0232804
UMLS CUI [3,1]
C0231199
UMLS CUI [3,2]
C0009429
received thoracic rt before
Description

Radiotherapy to thorax

Data type

boolean

Alias
UMLS CUI [1]
C4038705
pregnant or breast-feeding women
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
present with active infection
Description

Communicable Disease

Data type

boolean

Alias
UMLS CUI [1]
C0009450
uncontrolled diabetes
Description

Diabetic - poor control

Data type

boolean

Alias
UMLS CUI [1]
C0421258
concurrent use of other anti-cancer agents
Description

Antineoplastic Agents

Data type

boolean

Alias
UMLS CUI [1]
C0003392
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Similar models

Eligibility Carcinoma, Non-Small Cell Lung NCT00973310

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
aged 18-70 years，
boolean
C0001779 (UMLS CUI [1])
Non-Small Cell Lung Carcinoma TNM clinical staging
Item
patients with stage iiia-iiib nsclc
boolean
C0007131 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
Hematologic function | White Blood Cell Count procedure | Platelet Count measurement | Liver function | Serum total bilirubin measurement | Renal function | Creatinine clearance measurement
Item
adequate hematologic (wbc and platelet counts within normal limits), hepatic (total bilirubin level <= two times the upper limit of normal), and renal (creatinine clearance >= 50ml/min) functions
boolean
C0221130 (UMLS CUI [1])
C0023508 (UMLS CUI [2])
C0032181 (UMLS CUI [3])
C0232741 (UMLS CUI [4])
C1278039 (UMLS CUI [5])
C0232804 (UMLS CUI [6])
C0373595 (UMLS CUI [7])
Chemotherapy Absent | Chemotherapy cycle Neoadjuvant Quantity
Item
no history of chemotherapy or less than 4 cycles neoadjuvant chemotherapy
boolean
C0392920 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C1302181 (UMLS CUI [2,1])
C0600558 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
Intolerance Chemoradiotherapy | Chemoradiotherapy Refused
Item
can not tolerate or refuse concurrent chemoradiotherapy
boolean
C0231199 (UMLS CUI [1,1])
C0436307 (UMLS CUI [1,2])
C0436307 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Radiotherapy to thorax Absent
Item
no history of thoracic rt
boolean
C4038705 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Informed Consent
Item
written informed consent obtained
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Cancer Other
Item
with other malignancy
boolean
C1707251 (UMLS CUI [1])
Cardiopulmonary disease Severe
Item
with severe cardiopulmonary disease
boolean
C0034072 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Liver Dysfunction | Renal function | Intolerance Combined Modality Therapy
Item
compromised liver or renal function that could not tolerate the combined therapy
boolean
C0086565 (UMLS CUI [1])
C0232804 (UMLS CUI [2])
C0231199 (UMLS CUI [3,1])
C0009429 (UMLS CUI [3,2])
Radiotherapy to thorax
Item
received thoracic rt before
boolean
C4038705 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or breast-feeding women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Communicable Disease
Item
present with active infection
boolean
C0009450 (UMLS CUI [1])
Diabetic - poor control
Item
uncontrolled diabetes
boolean
C0421258 (UMLS CUI [1])
Antineoplastic Agents
Item
concurrent use of other anti-cancer agents
boolean
C0003392 (UMLS CUI [1])
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