ID

44055

Beschrijving

Study documentation part: Pre-Treatment This is a phase III study of BMS-354825 in subjects with chronic myelogenous leukemia in accelerated phase, or in myeloid or lymphoid blast phase or with Philadelphia chromosome positive (Ph+) acute lymphoblastic leukemia who are resistant or intolerant to imatinib mesylate (Gleevec).Trial Number: NCT00123487. Drug: dasatinib. Phase 3.

Trefwoorden

Versies (4)
  1. 06-07-15 06-07-15 -
  2. 06-08-15 06-08-15 -
  3. 15-03-21 15-03-21 - Dr. rer. medic Philipp Neuhaus
  4. 20-09-21 20-09-21 -
Geüploaded op

20 september 2021

DOI

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Licentie

Creative Commons BY-NC 3.0 Legacy
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Advanced Chronic Myelogenous Leukemia (CML) NCT00123487 – Pre-Treatment

Engels

Pre- treatment status

8 Formulieren  
PRE-TREATMENT STATUS
Beschrijving

PRE-TREATMENT STATUS

Will the subject enter the treatment phase of this study?
Beschrijving

WILL THE SUBJECT ENTER THE TREATMENT PHASE OF THIS STUDY ?

Datatype

boolean

PRIMARY REASON FOR NOT ENTERING THE TREATMENT PHASE OF THIS STUDY (Fill only if study entry is denied)
Beschrijving

PRIMARY REASON FOR NOT ENTERING THE TREATMENT PHASE OF THIS STUDY (Fill only if study entry is denied)

Adverse event:
Beschrijving

ADVERSE EVENT

Datatype

boolean

Alias
UMLS CUI-1
C0877248
Subject withdrew consent (specify):
Beschrijving

SUBJECT WITHDREW CONSENT (SPECIFY)

Datatype

text

Alias
UMLS CUI-1
C0514044
UMLS CUI-2
C0805443
Death:
Beschrijving

DEATH

Datatype

boolean

Alias
UMLS CUI-1
C0011065
Lost to Follow-up (Date of last contact):
Beschrijving

LOST TO FOLLOW-UP (DATE OF LAST CONTACT)

Datatype

date

Alias
UMLS CUI-1
C0011008
Poor/ Non- compliance (specify):
Beschrijving

Poor/ Non- compliance (specify)

Datatype

text

Alias
UMLS CUI-1
C1321605
Pregnancy:
Beschrijving

PREGNANCY

Datatype

boolean

Alias
UMLS CUI-1
C0549206
Subject no longer meets study criteria (specify):
Beschrijving

SUBJECT NO LONGER MEETS STUDY CRITERIA (SPECIFY)

Datatype

text

Administrative reason by sponsor:
Beschrijving

ADMINISTRATIVE REASON BY SPONSOR

Datatype

boolean

Others (Specify):
Beschrijving

Others (Specify)

Datatype

text

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Similar models

Pre- treatment status

8 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
PRE-TREATMENT STATUS
PRE-TREATMENT STATUS
Item
Will the subject enter the treatment phase of this study?
boolean
Item Group
PRIMARY REASON FOR NOT ENTERING THE TREATMENT PHASE OF THIS STUDY (Fill only if study entry is denied)
ADVERSE EVENT
Item
Adverse event:
boolean
C0877248 (UMLS CUI-1)
CONSENT
Item
Subject withdrew consent (specify):
text
C0514044 (UMLS CUI-1)
C0805443 (UMLS CUI-2)
DEATH
Item
Death:
boolean
C0011065 (UMLS CUI-1)
Date
Item
Lost to Follow-up (Date of last contact):
date
C0011008 (UMLS CUI-1)
COMPLIANCE
Item
Poor/ Non- compliance (specify):
text
C1321605 (UMLS CUI-1)
PREGNANCY
Item
Pregnancy:
boolean
C0549206 (UMLS CUI-1)
STUDY CRITERIA
Item
Subject no longer meets study criteria (specify):
text
ADMINISTRATIVE REASON BY SPONSOR
Item
Administrative reason by sponsor:
boolean
Others
Item
Others (Specify):
text
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