ID

31016

Beschreibung

A Multicenter Trial Comparing Multi-course Chemotherapy in Locoregionally Advanced Nasopharyngeal Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00705627

Link

https://clinicaltrials.gov/show/NCT00705627

Stichworte

  1. 10.07.18 10.07.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

10. Juli 2018

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Nasopharyngeal Carcinoma NCT00705627

Eligibility Nasopharyngeal Carcinoma NCT00705627

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with newly histologically confirmed nasopharyngeal carcinoma, including who ii or iii
Beschreibung

Nasopharyngeal carcinoma WHO tumor classification Grade

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2931822
UMLS CUI [1,2]
C1301142
UMLS CUI [1,3]
C0441800
original clinical stage must be t4 or n2-3 (uicc 2002)
Beschreibung

TNM clinical staging

Datentyp

boolean

Alias
UMLS CUI [1]
C3258246
male and no pregnant female
Beschreibung

Gender | Pregnancy Absent

Datentyp

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C0032961
UMLS CUI [2,2]
C0332197
age between 18-60
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
wbc ≥4,000/mm3 and plt ≥ 100,000/mm3
Beschreibung

White Blood Cell Count procedure | Platelet Count measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0023508
UMLS CUI [2]
C0032181
with normal liver function test (alt、ast≤2.5×uln)
Beschreibung

Liver function tests normal | Alanine aminotransferase measurement | Aspartate aminotransferase measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0438235
UMLS CUI [2]
C0201836
UMLS CUI [3]
C0201899
with normal renal function test (creatinine ≤ 1.5×uln)
Beschreibung

Renal function tests normal | Creatinine measurement, serum

Datentyp

boolean

Alias
UMLS CUI [1]
C0438262
UMLS CUI [2]
C0201976
performance status scale ecog grade 0,1
Beschreibung

ECOG performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
without radiotherapy or chemotherapy
Beschreibung

Therapeutic radiology procedure Absent | Chemotherapy Absent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C0332197
patients must give signed informed consent
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients have evidence of relapse or distant metastasis
Beschreibung

Recurrent disease | Distant metastatis

Datentyp

boolean

Alias
UMLS CUI [1]
C0277556
UMLS CUI [2]
C1269798
the presence of uncontrolled life-threatening illness
Beschreibung

Life threatening illness Uncontrolled

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3846017
UMLS CUI [1,2]
C0205318
receiving other ways of anti-cancer therapy
Beschreibung

Cancer treatment Other

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C0205394
receiving radiotherapy or chemotherapy
Beschreibung

Therapeutic radiology procedure | Chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1]
C1522449
UMLS CUI [2]
C0392920
investigator consider the patients can't finish the whole study
Beschreibung

Patients Completion of clinical trial Unlikely

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C2732579
UMLS CUI [1,3]
C0750558

Ähnliche Modelle

Eligibility Nasopharyngeal Carcinoma NCT00705627

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Nasopharyngeal carcinoma WHO tumor classification Grade
Item
patients with newly histologically confirmed nasopharyngeal carcinoma, including who ii or iii
boolean
C2931822 (UMLS CUI [1,1])
C1301142 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
TNM clinical staging
Item
original clinical stage must be t4 or n2-3 (uicc 2002)
boolean
C3258246 (UMLS CUI [1])
Gender | Pregnancy Absent
Item
male and no pregnant female
boolean
C0079399 (UMLS CUI [1])
C0032961 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Age
Item
age between 18-60
boolean
C0001779 (UMLS CUI [1])
White Blood Cell Count procedure | Platelet Count measurement
Item
wbc ≥4,000/mm3 and plt ≥ 100,000/mm3
boolean
C0023508 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
Liver function tests normal | Alanine aminotransferase measurement | Aspartate aminotransferase measurement
Item
with normal liver function test (alt、ast≤2.5×uln)
boolean
C0438235 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
C0201899 (UMLS CUI [3])
Renal function tests normal | Creatinine measurement, serum
Item
with normal renal function test (creatinine ≤ 1.5×uln)
boolean
C0438262 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
ECOG performance status
Item
performance status scale ecog grade 0,1
boolean
C1520224 (UMLS CUI [1])
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
patients must give signed informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Recurrent disease | Distant metastatis
Item
patients have evidence of relapse or distant metastasis
boolean
C0277556 (UMLS CUI [1])
C1269798 (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])
Cancer treatment Other
Item
receiving other ways of anti-cancer therapy
boolean
C0920425 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Therapeutic radiology procedure | Chemotherapy
Item
receiving radiotherapy or chemotherapy
boolean
C1522449 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
Patients Completion of clinical trial Unlikely
Item
investigator consider the patients can't finish the whole study
boolean
C0030705 (UMLS CUI [1,1])
C2732579 (UMLS CUI [1,2])
C0750558 (UMLS CUI [1,3])

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