ID

34418

Beskrivning

Endostar Combination With Chemotherapy for the Metastatic Nasopharyngeal Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT01612286

Länk

https://clinicaltrials.gov/show/NCT01612286

Nyckelord

  1. 2019-01-17 2019-01-17 -
  2. 2020-03-27 2020-03-27 - Sarah Riepenhausen
Rättsinnehavare

GSK group of companies

Uppladdad den

17 januari 2019

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Nasopharyngeal Carcinoma NCT01612286

Eligibility Nasopharyngeal Carcinoma NCT01612286

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosed metastatic npc patient who have received radiotherapy or chemoradiotherapy with an at least 6 months interval
Beskrivning

ID.1

Datatyp

boolean

have measurable lesions
Beskrivning

ID.2

Datatyp

boolean

no dysfunction of the major organs
Beskrivning

ID.3

Datatyp

boolean

can understand this study and give a signed informed consent certificates
Beskrivning

ID.4

Datatyp

boolean

without a history of allergic reaction to the biological agents
Beskrivning

ID.5

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating women; women of child-bearing age without contraception
Beskrivning

ID.6

Datatyp

boolean

with a serious infection or dysfunction of the major organs
Beskrivning

ID.7

Datatyp

boolean

have taken other antitumor drugs during the period of 30 days ahead of this clinical trial
Beskrivning

ID.8

Datatyp

boolean

allergic to the escherichia coli preparations
Beskrivning

ID.9

Datatyp

boolean

cann't understand this study and give a signed informed consent certificates
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Nasopharyngeal Carcinoma NCT01612286

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
diagnosed metastatic npc patient who have received radiotherapy or chemoradiotherapy with an at least 6 months interval
boolean
ID.2
Item
have measurable lesions
boolean
ID.3
Item
no dysfunction of the major organs
boolean
ID.4
Item
can understand this study and give a signed informed consent certificates
boolean
ID.5
Item
without a history of allergic reaction to the biological agents
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
pregnant or lactating women; women of child-bearing age without contraception
boolean
ID.7
Item
with a serious infection or dysfunction of the major organs
boolean
ID.8
Item
have taken other antitumor drugs during the period of 30 days ahead of this clinical trial
boolean
ID.9
Item
allergic to the escherichia coli preparations
boolean
ID.10
Item
cann't understand this study and give a signed informed consent certificates
boolean

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