ID

28392

Beskrivning

Phase II Study of AS1411 Combined With Cytarabine to Treat Acute Myeloid Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00512083

Länk

https://clinicaltrials.gov/show/NCT00512083

Nyckelord

  1. 2017-06-29 2017-06-29 -
  2. 2018-01-10 2018-01-10 - Julian Varghese
  3. 2018-01-10 2018-01-10 - Julian Varghese
Rättsinnehavare

Antisoma Research

Uppladdad den

10 januari 2018

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Leukemia, Myeloid NCT00512083

Eligibility Leukemia, Myeloid NCT00512083

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
primary refractory or relapsed aml
Beskrivning

Primary refractory or relapsed aml

Datatyp

boolean

Alias
UMLS CUI [1]
C0278780
confirmed diagnosis of aml (de novo or secondary) as defined by who classification
Beskrivning

Confirmed diagnosis aml

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0023467
UMLS CUI [1,2]
C0011900
aged at least 18 years
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
initial diagnosis of acute promyelocytic leukemia as defined by french-american-british criteria (bennett 1976)
Beskrivning

Acute Promyelocytic Leukemia

Datatyp

boolean

Alias
UMLS CUI [1]
C0023487
patient in blast crisis stage of chronic myeloid leukemia
Beskrivning

Blast crisis stage of chronic myeloid leukemia

Datatyp

boolean

Alias
UMLS CUI [1]
C0919644
received high-dose cytarabine (total cumulative dose of >6g/m sq)in last 6 months
Beskrivning

High-dose cytarabine

Datatyp

boolean

Alias
UMLS CUI [1]
C0010711
interval of <6 months between first onset of last complete remission and current relapse
Beskrivning

Interval first onset of last complete remission and current relapse

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0677874
UMLS CUI [1,2]
C0035020
those with primary refractory leukemia who have received more than three previous induction cycles
Beskrivning

Primary refractory leukemia

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0857127
UMLS CUI [1,2]
C0392920
relapsed patients who have received more than three previous treatment regimens
Beskrivning

Relapsed patients, more than three previous treatment regimens

Datatyp

boolean

Alias
UMLS CUI [1]
C0392920

Similar models

Eligibility Leukemia, Myeloid NCT00512083

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Primary refractory or relapsed aml
Item
primary refractory or relapsed aml
boolean
C0278780 (UMLS CUI [1])
Confirmed diagnosis aml
Item
confirmed diagnosis of aml (de novo or secondary) as defined by who classification
boolean
C0023467 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
Age
Item
aged at least 18 years
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Acute Promyelocytic Leukemia
Item
initial diagnosis of acute promyelocytic leukemia as defined by french-american-british criteria (bennett 1976)
boolean
C0023487 (UMLS CUI [1])
Blast crisis stage of chronic myeloid leukemia
Item
patient in blast crisis stage of chronic myeloid leukemia
boolean
C0919644 (UMLS CUI [1])
High-dose cytarabine
Item
received high-dose cytarabine (total cumulative dose of >6g/m sq)in last 6 months
boolean
C0010711 (UMLS CUI [1])
Interval first onset of last complete remission and current relapse
Item
interval of <6 months between first onset of last complete remission and current relapse
boolean
C0677874 (UMLS CUI [1,1])
C0035020 (UMLS CUI [1,2])
Primary refractory leukemia
Item
those with primary refractory leukemia who have received more than three previous induction cycles
boolean
C0857127 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
Relapsed patients, more than three previous treatment regimens
Item
relapsed patients who have received more than three previous treatment regimens
boolean
C0392920 (UMLS CUI [1])

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