ID
44592
Descripción
ODM derived from http://clinicaltrials.gov/show/NCT01018069
Link
http://clinicaltrials.gov/show/NCT01018069
Palabras clave
Versiones (3)
- 7/12/13 7/12/13 - Martin Dugas
- 17/4/14 17/4/14 - Julian Varghese
- 27/9/21 27/9/21 -
Subido en
27 de septiembre de 2021
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY 4.0
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Eligibility NCT01018069 Leukemia
Eligibility
- StudyEvent: Eligibility
Descripción
Ausschlusskriterien
Alias
- UMLS CUI 2011AA
- CL425201
Descripción
Clinical evidence of ongoing grade 3 or 4 non-hematological toxicities from the initial standard dose cytarabine-based induction chemotherapy
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0549178
- UMLS CUI 2011AA
- C1518422
- UMLS CUI 2011AA
- C0205488
- SNOMED CT 2011_0131
- 57407000
- UMLS CUI 2011AA
- C2826262
- UMLS CUI 2011AA
- C0205449
- SNOMED CT 2011_0131
- 421291004
- UMLS CUI 2011AA
- C0205450
- SNOMED CT 2011_0131
- 9362000
- UMLS CUI 2011AA
- C0010711
- SNOMED CT 2011_0131
- 89265009
- UMLS CUI 2011AA
- C0205263
- SNOMED CT 2011_0131
- 16404004
- UMLS CUI 2011AA
- C0392920
- SNOMED CT 2011_0131
- 150415003
Descripción
Patients with a prior history of peripheral neuropathy of grade >= 2.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- CL421546
- SNOMED CT 2011_0131
- 392521001
- UMLS CUI 2011AA
- C0031117
- MedDRA 14.1
- 10029331
- ICD-10-CM Version 2010
- G64
- ICD-9-CM Version 2011
- 350-359.99
- UMLS CUI 2011AA
- C0441800
- SNOMED CT 2011_0131
- 258349007
- LOINC Version 232
- MTHU003112
Descripción
Clinical evidence of active CNS leukemic involvement.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0205177
- SNOMED CT 2011_0131
- 55561003
- UMLS CUI 2011AA
- C1332884
- SNOMED CT 2011_0131
- 10067299
- UMLS CUI 2011AA
- C1314939
- SNOMED CT 2011_0131
- 248448006
Descripción
Active and uncontrolled infection. Patients with an infection who are under active treatment with antibiotics and whose infections are controlled may be entered to the study.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0009450
Descripción
Current evidence of invasive fungal infection (blood or tissue culture).
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0205281
- SNOMED CT 2011_0131
- 10179008
- UMLS CUI 2011AA
- C0026946
- SNOMED CT 2011_0131
- 3218000
- MedDRA 14.1
- 10017533
- ICD-10-CM Version 2010
- B35-B49
- ICD-9-CM Version 2011
- 110-118.99
- UMLS CUI 2011AA
- C0200949
- SNOMED CT 2011_0131
- 30088009
- MedDRA 14.1
- 10005485
- ICD-9-CM Version 2011
- 90.52
- UMLS CUI 2011AA
- C0040284
- SNOMED CT 2011_0131
- 77601007
Descripción
Current evidence of an active second malignancy except for non-melanoma skin cancer.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0205177
- SNOMED CT 2011_0131
- 55561003
- UMLS CUI 2011AA
- C0085183
- UMLS CUI 2011AA
- C1554961
- HL7 V3 2006_05
- E
- UMLS CUI 2011AA
- C0699893
- MedDRA 14.1
- 10040810
Descripción
Uncontrolled medical problems, unrelated to the malignancy, or of sufficient severity that in the opinion of the investigator, impair a patient's ability to give informed consent or unacceptably reduce the safety of the proposed treatment.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C1522577
Descripción
Neurological or psychiatric disorders that would interfere with consent or study follow-up.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0021430
Descripción
Known or suspected intolerance or hypersensitivity to the study drugs [or closely related compounds] or any of their stated ingredients. Study drugs being the antisense, cytarabine and idarubicin.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C1744706
- UMLS CUI 2011AA
- C0020517
- SNOMED CT 2011_0131
- 418634005
- ICD-10-CM Version 2010
- T78.40
- UMLS CUI 2011AA
- C0304229
- SNOMED CT 2011_0131
- 902003
- UMLS CUI 2011AA
- CL414967
- UMLS CUI 2011AA
- C0079925
- UMLS CUI 2011AA
- C0010711
- SNOMED CT 2011_0131
- 89265009
- UMLS CUI 2011AA
- C0020789
- SNOMED CT 2011_0131
- 372539000
Descripción
History of alcohol or other substance abuse within the last year.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0085762
Descripción
Use of another investigational agent within the last 14 days prior to enrolment. Patients who have received a previous antisense agent in the last 90 days will be excluded.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C1524063
- SNOMED CT 2011_0131
- 260676000
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- C0013230
- UMLS CUI 2011AA
- C0205448
- SNOMED CT 2011_0131
- 19338005
- UMLS CUI 2011AA
- C0439230
- SNOMED CT 2011_0131
- 258705008
- HL7 V3 2006_05
- WK
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C1516879
Descripción
Female patients who are pregnant, lactating, or with a positive pregnancy test at screening must be excluded.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0086287
- SNOMED CT 2011_0131
- 248152002
- HL7 V3 2006_05
- F
- UMLS CUI 2011AA
- C0549206
- MedDRA 14.1
- 10036586
- UMLS CUI 2011AA
- C2828358
- UMLS CUI 2011AA
- C0240802
- SNOMED CT 2011_0131
- 250423000
- MedDRA 14.1
- 10036575
- UMLS CUI 2011AA
- C1409616
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