ID
13564
Descripción
Study of Clofarabine & Cytosine Arabinoside Therapy for Older Adults With Acute Myeloid Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00081822
Link
https://clinicaltrials.gov/show/NCT00081822
Palabras clave
Versiones (1)
- 16/2/16 16/2/16 -
Titular de derechos de autor
CC BY-NC 3.0
Subido en
16 de febrero de 2016
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC 3.0
Comentarios del modelo :
Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.
Comentarios de grupo de elementos para :
Comentarios del elemento para :
Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.
Eligibility Acute Myeloid Leukemia NCT00081822
Eligibility Acute Myeloid Leukemia NCT00081822
- StudyEvent: Eligibility
Descripción
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Descripción
patients with pre-existing myelodysplastic syndrome, or with antecedent hematologic disorder of >3 months duration, will be excluded. those with concomitant myelodysplasia/trilineage dysplasia noted at the time of diagnosis of aml will be eligible 74
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C3463824
- UMLS CUI [2]
- C0018939
Descripción
have secondary aml (aml following chemotherapy or radiation therapy).
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0280449
Descripción
have an active, uncontrolled systemic infection considered opportunistic, life threatening, or clinically significant at the time of treatment.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0009488
Descripción
have a psychiatric disorder(s) that would interfere with consent, study participation or follow-up.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Descripción
are receiving other chemotherapy or corticosteroids (unless the latter is administered at a low dose for pre-medication purposes or for the treatment of chronic conditions - e.g., rheumatoid arthritis).
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0392920
- UMLS CUI [2]
- C0001617
Descripción
have received prior treatment for leukemia. patients who have received growth factors, cytokine support, leukapheresis, hydroxyurea, or cranial irradiation will be allowed but must discontinue treatment at least 24 hours prior to beginning treatment with clofarabine. if used, hydroxyurea must be discontinued 48 hours prior to the initiation of chemotherapy.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1514463
- UMLS CUI [2]
- C0018284
- UMLS CUI [3]
- C0199974
- UMLS CUI [4]
- C0023416
- UMLS CUI [5]
- C0020402
- UMLS CUI [6]
- C0079172
Descripción
have any other severe concurrent disease (severe coronary artery disease (nyha class >ii), significant neurological disorder, uncontrolled diabetes, etc.), which, in the judgment of the investigator, would make the patient inappropriate for entry into this study.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1321605
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Descripción
have active central nervous system involvement with leukemia.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1332884
Descripción
other malignancy within the past year, with the exception of basal cell or non-metastatic squamous cell carcinoma of the skin
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0006826
Similar models
Eligibility Acute Myeloid Leukemia NCT00081822
- StudyEvent: Eligibility
C0023487 (UMLS CUI [2])
C3688712 (UMLS CUI [3])
C1515708 (UMLS CUI [4])
C2825131 (UMLS CUI [5])
C0032961 (UMLS CUI [2])
C0700589 (UMLS CUI [3])
C1278039 (UMLS CUI [2])
C0201899 (UMLS CUI [3])
C0201836 (UMLS CUI [4])
C0018939 (UMLS CUI [2])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0001617 (UMLS CUI [2])
C0018284 (UMLS CUI [2])
C0199974 (UMLS CUI [3])
C0023416 (UMLS CUI [4])
C0020402 (UMLS CUI [5])
C0079172 (UMLS CUI [6])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])