ID

36559

Description

A Trial On 4 Cycles Of Neoadjuvant Chemotherapy Plus Concurrent Chemoradiation In N2-3 Nasopharyngeal Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT02512315

Link

https://clinicaltrials.gov/show/NCT02512315

Keywords

Versions (1)
  1. 5/21/19 5/21/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

May 21, 2019

DOI

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License

Creative Commons BY 4.0
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Eligibility Nasopharyngeal Carcinoma NCT02512315

English

Eligibility Nasopharyngeal Carcinoma NCT02512315

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with pathological diagnosis of nasopharyngeal carcinoma
Description

Nasopharyngeal carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C2931822
union internationale contre le cancer/american joint cancer committee (uicc/ajcc) 2010 stage t1-4 n2-3 m0 through magnetic resonance imaging of head and neck, whole-body bone scan and thoracoabdominal computed tomography
Description

TNM clinical staging MRI of head and neck | TNM clinical staging Whole body isotopic bone scan | TNM clinical staging CT of chest and abdomen

Data type

boolean

Alias
UMLS CUI [1,1]
C3258246
UMLS CUI [1,2]
C3839598
UMLS CUI [2,1]
C3258246
UMLS CUI [2,2]
C3863086
UMLS CUI [3,1]
C3258246
UMLS CUI [3,2]
C1630402
male or female with age no older than 70 years old
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
karnofsky performance scores ≥ 80
Description

Karnofsky Performance Status

Data type

boolean

Alias
UMLS CUI [1]
C0206065
expected survival ≥ 3 months
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with distant metastasis before or during radiotherapy
Description

Distant metastasis | Therapeutic radiology procedure

Data type

boolean

Alias
UMLS CUI [1]
C1269798
UMLS CUI [2]
C1522449
severe dysfunction of heart, lung, liver, kidney or hematopoietic system
Description

Cardiac dysfunction Severe | Pulmonary Dysfunction Severe | Liver Dysfunction Severe | Renal dysfunction Severe | Hematopoietic System Dysfunction Severe

Data type

boolean

Alias
UMLS CUI [1,1]
C3277906
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C1709770
UMLS CUI [2,2]
C0205082
UMLS CUI [3,1]
C0086565
UMLS CUI [3,2]
C0205082
UMLS CUI [4,1]
C3279454
UMLS CUI [4,2]
C0205082
UMLS CUI [5,1]
C0018957
UMLS CUI [5,2]
C3887504
UMLS CUI [5,3]
C0205082
severe neurological, mental or endocrine diseases
Description

Nervous system disorder Severe | Mental disorder Severe | Endocrine System Disease Severe

Data type

boolean

Alias
UMLS CUI [1,1]
C0027765
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0004936
UMLS CUI [2,2]
C0205082
UMLS CUI [3,1]
C0014130
UMLS CUI [3,2]
C0205082
history of other malignancies
Description

Cancer Other

Data type

boolean

Alias
UMLS CUI [1]
C1707251
prior chemotherapy, radiotherapy or application of monoclonal antibodies
Description

Prior Chemotherapy | Prior radiation therapy | Monoclonal Antibodies

Data type

boolean

Alias
UMLS CUI [1]
C1514457
UMLS CUI [2]
C0279134
UMLS CUI [3]
C0003250
patients participated in clinical trials of other drugs within last 3 months
Description

Study Subject Participation Status | Investigational New Drugs

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
pregnant or lactating women
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
those who are considered by the researchers unsuitable to participate
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 Nasopharyngeal Carcinoma NCT02512315

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Nasopharyngeal carcinoma
Item
patients with pathological diagnosis of nasopharyngeal carcinoma
boolean
C2931822 (UMLS CUI [1])
TNM clinical staging MRI of head and neck | TNM clinical staging Whole body isotopic bone scan | TNM clinical staging CT of chest and abdomen
Item
union internationale contre le cancer/american joint cancer committee (uicc/ajcc) 2010 stage t1-4 n2-3 m0 through magnetic resonance imaging of head and neck, whole-body bone scan and thoracoabdominal computed tomography
boolean
C3258246 (UMLS CUI [1,1])
C3839598 (UMLS CUI [1,2])
C3258246 (UMLS CUI [2,1])
C3863086 (UMLS CUI [2,2])
C3258246 (UMLS CUI [3,1])
C1630402 (UMLS CUI [3,2])
Age
Item
male or female with age no older than 70 years old
boolean
C0001779 (UMLS CUI [1])
Karnofsky Performance Status
Item
karnofsky performance scores ≥ 80
boolean
C0206065 (UMLS CUI [1])
Life Expectancy
Item
expected survival ≥ 3 months
boolean
C0023671 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Distant metastasis | Therapeutic radiology procedure
Item
patients with distant metastasis before or during radiotherapy
boolean
C1269798 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
Cardiac dysfunction Severe | Pulmonary Dysfunction Severe | Liver Dysfunction Severe | Renal dysfunction Severe | Hematopoietic System Dysfunction Severe
Item
severe dysfunction of heart, lung, liver, kidney or hematopoietic system
boolean
C3277906 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C1709770 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0086565 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C3279454 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0018957 (UMLS CUI [5,1])
C3887504 (UMLS CUI [5,2])
C0205082 (UMLS CUI [5,3])
Nervous system disorder Severe | Mental disorder Severe | Endocrine System Disease Severe
Item
severe neurological, mental or endocrine diseases
boolean
C0027765 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0004936 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0014130 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
Cancer Other
Item
history of other malignancies
boolean
C1707251 (UMLS CUI [1])
Prior Chemotherapy | Prior radiation therapy | Monoclonal Antibodies
Item
prior chemotherapy, radiotherapy or application of monoclonal antibodies
boolean
C1514457 (UMLS CUI [1])
C0279134 (UMLS CUI [2])
C0003250 (UMLS CUI [3])
Study Subject Participation Status | Investigational New Drugs
Item
patients participated in clinical trials of other drugs within last 3 months
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status Inappropriate
Item
those who are considered by the researchers unsuitable to participate
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
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