ID
5123
Descripción
ODM derived from http://clinicaltrials.gov/show/NCT01295307
Link
http://clinicaltrials.gov/show/NCT01295307
Palabras clave
Versiones (3)
- 19/3/13 19/3/13 - Martin Dugas
- 19/4/14 19/4/14 - Julian Varghese
- 20/9/21 20/9/21 -
Subido en
19 de abril de 2014
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY 4.0
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Eligibility NCT01295307 Acute Myeloid Leukemia
Eligibility
- StudyEvent: Eligibility
Descripción
Ausschlusskriterien
Descripción
For refractory disease, more than two prior induction chemotherapies or more than one prior salvage chemotherapy containing high-dose cytarabine (cumulative dose of cytarabine >= 5 g/m2).
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C1514815
- UMLS CUI 2011AA
- C0439093
- SNOMED CT 2011_0131
- 276140008
- HL7 V3 2006_05
- GT
- UMLS CUI 2011AA
- C0205448
- SNOMED CT 2011_0131
- 19338005
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C3179010
- UMLS CUI 2011AA
- C0205447
- SNOMED CT 2011_0131
- 38112003
- UMLS CUI 2011AA
- C0085405
- MedDRA 14.1
- 10068833
- UMLS CUI 2011AA
- C0444956
- SNOMED CT 2011_0131
- 261829003
- UMLS CUI 2011AA
- C0010711
- SNOMED CT 2011_0131
- 89265009
Descripción
Second or higher relapse. Patients who received hypomethylating agents like azacytidine or decitabine as a treatment of first relapse, respond and relapse later on may be included.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0439093
- SNOMED CT 2011_0131
- 276140008
- HL7 V3 2006_05
- GT
- UMLS CUI 2011AA
- C0205447
- SNOMED CT 2011_0131
- 38112003
- UMLS CUI 2011AA
- C0277556
- SNOMED CT 2011_0131
- 58184002
- UMLS CUI 2011AA
- C1514756
- UMLS CUI 2011AA
- C1254351
- UMLS CUI 2011AA
- CL414898
- UMLS CUI 2011AA
- C2613367
- UMLS CUI 2011AA
- C0004475
- SNOMED CT 2011_0131
- 412329008
- UMLS CUI 2011AA
- C0049065
- SNOMED CT 2011_0131
- 420517007
- UMLS CUI 2011AA
- C0332149
- SNOMED CT 2011_0131
- 371930009
- UMLS CUI 2011AA
- C1302261
- SNOMED CT 2011_0131
- 399223003
Descripción
Acute promyelocytic leukemia with t(15;17)(q22;q12) molecular detection or (PML/RARalpha).
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0023487
- SNOMED CT 2011_0131
- 110004001
- MedDRA 14.1
- 10001019
- ICD-10-CM Version 2010
- C92.4
- UMLS CUI 2011AA
- C1515724
- UMLS CUI 2011AA
- CL414625
- UMLS CUI 2011AA
- C1511790
- UMLS CUI 2011AA
- C0279625
Descripción
Central nervous system involvement (i.e. WBC >= 5/microL in cerebrospinal fluid with blasts present on cytospin).
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0449389
- SNOMED CT 2011_0131
- 260766009
- UMLS CUI 2011AA
- C0023508
- SNOMED CT 2011_0131
- 767002
- MedDRA 14.1
- 10047939
- UMLS CUI 2011AA
- C1271796
- SNOMED CT 2011_0131
- 391308009
- UMLS CUI 2011AA
- C0150312
- SNOMED CT 2011_0131
- 52101004
- UMLS CUI 2011AA
- C0368761
- SNOMED CT 2011_0131
- 312256009
- LOINC Version 232
- MTHU005201
Descripción
Prior allogeneic HCT
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C2242529
- SNOMED CT 2011_0131
- 288556008
- MedDRA 14.1
- 10067862
Descripción
Autologous transplantation within 100 days prior to start of study treatment
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0040736
- SNOMED CT 2011_0131
- 53088000
- MedDRA 14.1
- 10064285
- UMLS CUI 2011AA
- C0332285
- SNOMED CT 2011_0131
- 18720000
- UMLS CUI 2011AA
- C1704407
- SNOMED CT 2011_0131
- 420528006
- UMLS CUI 2011AA
- C0439228
- SNOMED CT 2011_0131
- 258703001
- HL7 V3 2006_05
- D
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C2348558
Descripción
Use of investigational agents or anticancer therapy within 10 days before study entry with the exception of hydroxyurea or low-dose cytarabine.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C1524063
- SNOMED CT 2011_0131
- 260676000
- UMLS CUI 2011AA
- C0013230
- UMLS CUI 2011AA
- C0920425
- UMLS CUI 2011AA
- C1554961
- HL7 V3 2006_05
- E
- UMLS CUI 2011AA
- C0020402
- SNOMED CT 2011_0131
- 56602009
- UMLS CUI 2011AA
- C0445550
- SNOMED CT 2011_0131
- 262459003
- UMLS CUI 2011AA
- C0010711
- SNOMED CT 2011_0131
- 89265009
Descripción
Have any other severe concurrent disease, or have a history of serious organ dysfunction or disease involving the heart, kidney, liver, or other organ system that may place the patient at undue risk to undergo transplantation.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0205420
- SNOMED CT 2011_0131
- 68405009
- UMLS CUI 2011AA
- C0012634
- SNOMED CT 2011_0131
- 64572001
- UMLS CUI 2011AA
- CL421546
- SNOMED CT 2011_0131
- 392521001
- UMLS CUI 2011AA
- C0349410
- SNOMED CT 2011_0131
- 251526004
- UMLS CUI 2011AA
- C0018799
- SNOMED CT 2011_0131
- 56265001
- MedDRA 14.1
- 10061024
- UMLS CUI 2011AA
- C0022658
- SNOMED CT 2011_0131
- 90708001
- MedDRA 14.1
- 10029151
- ICD-10-CM Version 2010
- N18.9
- UMLS CUI 2011AA
- C0023895
- SNOMED CT 2011_0131
- 235856003
- MedDRA 14.1
- 10024670
- ICD-10-CM Version 2010
- K76.9
- ICD-9-CM Version 2011
- 573.9
- UMLS CUI 2011AA
- C0012634
- SNOMED CT 2011_0131
- 64572001
- UMLS CUI 2011AA
- C0460002
- SNOMED CT 2011_0131
- 91689009
Descripción
Patients with known refractoriness to platelet support.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0030705
- SNOMED CT 2011_0131
- 116154003
- UMLS CUI 2011AA
- C0205269
- SNOMED CT 2011_0131
- 20646008
- UMLS CUI 2011AA
- C0005821
- SNOMED CT 2011_0131
- 16378004
- LOINC Version 232
- MTHU002432
- UMLS CUI 2011AA
- C1521721
Descripción
Patients with a systemic fungal, bacterial, viral, or other infection not controlled (defined as exhibiting ongoing signs/symptoms related to the infection and without improvement, despite appropriate antibiotics or other treatment).
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0205373
- SNOMED CT 2011_0131
- 31099001
- 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
- C0004623
- SNOMED CT 2011_0131
- 87628006
- MedDRA 14.1
- 10060945
- ICD-10-CM Version 2010
- A49.9
- UMLS CUI 2011AA
- C0042769
- SNOMED CT 2011_0131
- 34014006
- MedDRA 14.1
- 10047461
- ICD-10-CM Version 2010
- B34.9
- UMLS CUI 2011AA
- C0205318
- SNOMED CT 2011_0131
- 19032002
- UMLS CUI 2011AA
- C0021311
- SNOMED CT 2011_0131
- 257551009
- MedDRA 14.1
- 10021789
Descripción
Pregnant or lactating patients.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0549206
- MedDRA 14.1
- 10036586
- UMLS CUI 2011AA
- C2828358
- UMLS CUI 2011AA
- C0030705
- SNOMED CT 2011_0131
- 116154003
Descripción
Any significant concurrent disease, illness, or psychiatric disorder that would compromise patient safety or compliance, interfere with consent, study participation, follow up, or interpretation of study results.
Tipo de datos
boolean
Alias
- UMLS CUI 2011AA
- C0205420
- SNOMED CT 2011_0131
- 68405009
- UMLS CUI 2011AA
- C0012634
- SNOMED CT 2011_0131
- 64572001
- UMLS CUI 2011AA
- C0004936
- SNOMED CT 2011_0131
- 74732009
- MedDRA 14.1
- 10037174
- ICD-10-CM Version 2010
- F99
- ICD-9-CM Version 2011
- 290-319.99
- UMLS CUI 2011AA
- C0221099
- SNOMED CT 2011_0131
- 260379002
- UMLS CUI 2011AA
- C1113679
- UMLS CUI 2011AA
- C0521102
- SNOMED CT 2011_0131
- 78235001
- UMLS CUI 2011AA
- C0525058
- UMLS CUI 2011AA
- C0459471
- SNOMED CT 2011_0131
- 280452008
- LOINC Version 232
- MTHU003869
- UMLS CUI 2011AA
- C0683954
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- StudyEvent: Eligibility
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56265001 (SNOMED CT 2011_0131)
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116154003 (SNOMED CT 2011_0131)
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