ID

31017

Description

Late-Course Accelerated Hyperfractionated IMRT for Locoregionally Advanced Nasopharyngeal Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00778908

Link

https://clinicaltrials.gov/show/NCT00778908

Keywords

Versions (1)
  1. 7/11/18 7/11/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

July 11, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Nasopharyngeal Carcinoma NCT00778908

English

Eligibility Nasopharyngeal Carcinoma NCT00778908

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically proven non-keratinizing or undifferentiated type nasopharyngeal carcinoma for primary treatment with curative intent
Description

First line treatment Curative intent Nasopharyngeal Nonkeratinizing Carcinoma | First line treatment Curative intent Undifferentiated carcinoma of nasopharynx

Data type

boolean

Alias
UMLS CUI [1,1]
C1708063
UMLS CUI [1,2]
C1276305
UMLS CUI [1,3]
C1334926
UMLS CUI [2,1]
C1708063
UMLS CUI [2,2]
C1276305
UMLS CUI [2,3]
C0279748
according to ajcc 2002 staging system, clinical stage must be ⅱb-ⅳb
Description

TNM clinical staging

Data type

boolean

Alias
UMLS CUI [1]
C3258246
age between 18-70
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
karnofsky performance status ≥70
Description

Karnofsky Performance Status

Data type

boolean

Alias
UMLS CUI [1]
C0206065
wbc ≥4,000/mm3, plt ≥ 100,000/mm3,serum creatinine ≤ 1.6 mg/dl
Description

White Blood Cell Count procedure | Platelet Count measurement | Creatinine measurement, serum

Data type

boolean

Alias
UMLS CUI [1]
C0023508
UMLS CUI [2]
C0032181
UMLS CUI [3]
C0201976
without radiotherapy or chemotherapy
Description

Therapeutic radiology procedure Absent | Chemotherapy Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C0332197
signed study-specific consent form prior to study entry
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with distant metastasis
Description

Distant metastasis

Data type

boolean

Alias
UMLS CUI [1]
C1269798
pregnant or lactating women
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
the presence of uncontrolled life-threatening illness
Description

Life threatening illness Uncontrolled

Data type

boolean

Alias
UMLS CUI [1,1]
C3846017
UMLS CUI [1,2]
C0205318
patients who received radiotherapy or chemotherapy previously
Description

Therapeutic radiology procedure | Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C1522449
UMLS CUI [2]
C0392920
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Similar models

Eligibility Nasopharyngeal Carcinoma NCT00778908

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
First line treatment Curative intent Nasopharyngeal Nonkeratinizing Carcinoma | First line treatment Curative intent Undifferentiated carcinoma of nasopharynx
Item
histologically proven non-keratinizing or undifferentiated type nasopharyngeal carcinoma for primary treatment with curative intent
boolean
C1708063 (UMLS CUI [1,1])
C1276305 (UMLS CUI [1,2])
C1334926 (UMLS CUI [1,3])
C1708063 (UMLS CUI [2,1])
C1276305 (UMLS CUI [2,2])
C0279748 (UMLS CUI [2,3])
TNM clinical staging
Item
according to ajcc 2002 staging system, clinical stage must be ⅱb-ⅳb
boolean
C3258246 (UMLS CUI [1])
Age
Item
age between 18-70
boolean
C0001779 (UMLS CUI [1])
Karnofsky Performance Status
Item
karnofsky performance status ≥70
boolean
C0206065 (UMLS CUI [1])
White Blood Cell Count procedure | Platelet Count measurement | Creatinine measurement, serum
Item
wbc ≥4,000/mm3, plt ≥ 100,000/mm3,serum creatinine ≤ 1.6 mg/dl
boolean
C0023508 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
C0201976 (UMLS CUI [3])
Therapeutic radiology procedure Absent | Chemotherapy Absent
Item
without radiotherapy or chemotherapy
boolean
C1522449 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Informed Consent
Item
signed study-specific consent form prior to study entry
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Distant metastasis
Item
patients with distant metastasis
boolean
C1269798 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Life threatening illness Uncontrolled
Item
the presence of uncontrolled life-threatening illness
boolean
C3846017 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Therapeutic radiology procedure | Chemotherapy
Item
patients who received radiotherapy or chemotherapy previously
boolean
C1522449 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
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