ID

12909

Beskrivning

Risk-Adapted Therapy of Acute Myeloid Leukemia of Adults (18-60 Years) According to the Cytogenetic Result; ODM derived from: https://clinicaltrials.gov/show/NCT00146120

Länk

https://clinicaltrials.gov/show/NCT00146120

Nyckelord

  1. 2016-01-06 2016-01-06 -
Rättsinnehavare

CC BY-NC 3.0

Uppladdad den

6 januari 2016

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Acute Myeloid Leukemia NCT00146120

Eligibility Acute Myeloid Leukemia NCT00146120

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with aml, de novo or secondary after myelodysplasy, or with therapy-induced aml after healed primary malignom; or refractory anemia with excess of blasts in transformation (raeb-t); the diagnosis must be confirmed morphological, cytochemical and with immunological phenotyping
Beskrivning

patients with aml, de novo or secondary after myelodysplasy, or with therapy-induced aml after healed primary malignom; or refractory anemia with excess of blasts in transformation (raeb-t); the diagnosis must be confirmed morphological, cytochemical and with immunological phenotyping

Datatyp

boolean

Alias
UMLS CUI [1]
C0023467
UMLS CUI [2]
C0002893
cytogenetical tests must be performed for each patient
Beskrivning

cytogenetical tests must be performed for each patient

Datatyp

boolean

Alias
UMLS CUI [1]
C0010802
age: 16 - 60 years
Beskrivning

age: 16 - 60 years

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
all patients have to be informed about the character of the study. written informed consent of each patient at study entry.
Beskrivning

all patients have to be informed about the character of the study. written informed consent of each patient at study entry.

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
organic insufficiency: insufficiency of the kidneys (crea > 1.5 x upper normal serum level), or insufficiency of the liver (bilirubin, sgot or ap > 2 x upper normal serum level) uncaused by the aml; severe obstruction or restrictive ventilation disorder, heart failure with a ejection fraction < 0.5
Beskrivning

organic insufficiency: insufficiency of the kidneys (crea > 1.5 x upper normal serum level), or insufficiency of the liver (bilirubin, sgot or ap > 2 x upper normal serum level) uncaused by the aml; severe obstruction or restrictive ventilation disorder, heart failure with a ejection fraction < 0.5

Datatyp

boolean

Alias
UMLS CUI [1]
C0201976
UMLS CUI [2]
C1278039
UMLS CUI [3]
C0035204
UMLS CUI [4]
C0232174
secondary malignom
Beskrivning

secondary malignom

Datatyp

boolean

Alias
UMLS CUI [1]
C0006826
other severe diseases
Beskrivning

other severe diseases

Datatyp

boolean

Alias
UMLS CUI [1]
C0009488
pregnancy
Beskrivning

pregnancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
participation in an concurrent clinical study
Beskrivning

participation in an concurrent clinical study

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Acute Myeloid Leukemia NCT00146120

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
patients with aml, de novo or secondary after myelodysplasy, or with therapy-induced aml after healed primary malignom; or refractory anemia with excess of blasts in transformation (raeb-t); the diagnosis must be confirmed morphological, cytochemical and with immunological phenotyping
Item
patients with aml, de novo or secondary after myelodysplasy, or with therapy-induced aml after healed primary malignom; or refractory anemia with excess of blasts in transformation (raeb-t); the diagnosis must be confirmed morphological, cytochemical and with immunological phenotyping
boolean
C0023467 (UMLS CUI [1])
C0002893 (UMLS CUI [2])
cytogenetical tests must be performed for each patient
Item
cytogenetical tests must be performed for each patient
boolean
C0010802 (UMLS CUI [1])
age: 16 - 60 years
Item
age: 16 - 60 years
boolean
C0001779 (UMLS CUI [1])
all patients have to be informed about the character of the study. written informed consent of each patient at study entry.
Item
all patients have to be informed about the character of the study. written informed consent of each patient at study entry.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
organic insufficiency: insufficiency of the kidneys (crea > 1.5 x upper normal serum level), or insufficiency of the liver (bilirubin, sgot or ap > 2 x upper normal serum level) uncaused by the aml; severe obstruction or restrictive ventilation disorder, heart failure with a ejection fraction < 0.5
Item
organic insufficiency: insufficiency of the kidneys (crea > 1.5 x upper normal serum level), or insufficiency of the liver (bilirubin, sgot or ap > 2 x upper normal serum level) uncaused by the aml; severe obstruction or restrictive ventilation disorder, heart failure with a ejection fraction < 0.5
boolean
C0201976 (UMLS CUI [1])
C1278039 (UMLS CUI [2])
C0035204 (UMLS CUI [3])
C0232174 (UMLS CUI [4])
secondary malignom
Item
secondary malignom
boolean
C0006826 (UMLS CUI [1])
other severe diseases
Item
other severe diseases
boolean
C0009488 (UMLS CUI [1])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
participation in an concurrent clinical study
Item
participation in an concurrent clinical study
boolean
C2348568 (UMLS CUI [1])

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