ID

13727

Descripción

Intensity Modulated Total Marrow Irradiation (IM-TMI) for Advanced Hematologic Malignancies; ODM derived from: https://clinicaltrials.gov/show/NCT00988013

Link

https://clinicaltrials.gov/show/NCT00988013

Palabras clave

Versiones (1)
  1. 1/3/16 1/3/16 -
Titular de derechos de autor

CC BY-NC 3.0

Subido en

1 de marzo 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.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

  • El más nuevo
  • Más antiguo
  • Popular
  • El más nuevo
    • El más nuevo
    • Más antiguo
    • Popular

Sin comentarios

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Acute Myeloid Leukemia NCT00988013

Inglés

Eligibility Acute Myeloid Leukemia NCT00988013

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with the following diseases: acute myeloid or lymphoblastic leukemia in first complete remission if poor prognosis documented by failure to response after initial induction chemotherapy, or cytogenetic, or molecular studies. acute leukemia in greater/equal second remission, or partial remission after chemotherapy. high grade non hodgkin's or hodgkin's lymphoma with marrow involvement resistant/ relapsed after second line therapy including high dose chemotherapy and autologous sct. cml in advanced or blastic phase. plasma cell leukemia.
Descripción

patients with the following diseases: acute myeloid or lymphoblastic leukemia in first complete remission if poor prognosis documented by failure to response after initial induction chemotherapy, or cytogenetic, or molecular studies. acute leukemia in greater/equal second remission, or partial remission after chemotherapy. high grade non hodgkin's or hodgkin's lymphoma with marrow involvement resistant/ relapsed after second line therapy including high dose chemotherapy and autologous sct. cml in advanced or blastic phase. plasma cell leukemia.

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023467
UMLS CUI [2]
C0023474
UMLS CUI [3]
C0023449
UMLS CUI [4]
C0019829
UMLS CUI [5]
C0024305
UMLS CUI [6]
C0023484
age 18-60 years.
Descripción

age 18-60 years.

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
karnofsky performance status of 70
Descripción

karnofsky performance status of 70

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0206065
adequate cardiac and pulmonary function. patients with decreased lvef less than/equal to 40% or dlco less than/equal to 50% of predicted will require clearance from cardiology or pulmonary services, respectively, prior to enrollment on this protocol.
Descripción

adequate cardiac and pulmonary function. patients with decreased lvef less than/equal to 40% or dlco less than/equal to 50% of predicted will require clearance from cardiology or pulmonary services, respectively, prior to enrollment on this protocol.

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0428772
UMLS CUI [2]
C1516251
serum creatinine less than/equal to 1.5 mg/dl or creatinine clearance greater than/equal to 50 ml/min .
Descripción

serum creatinine less than/equal to 1.5 mg/dl or creatinine clearance greater than/equal to 50 ml/min .

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0201976
UMLS CUI [2]
C0373595
serum bilirubin 2.0 mg/dl, sgpt less than/equal to 3 times the upper limit of normal
Descripción

serum bilirubin 2.0 mg/dl, sgpt less than/equal to 3 times the upper limit of normal

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1278039
UMLS CUI [2]
C0201836
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
life expectancy is severely limited by concomitant illness.
Descripción

life expectancy is severely limited by concomitant illness.

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0023671
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
evidence of chronic active hepatitis or cirrhosis
Descripción

evidence of chronic active hepatitis or cirrhosis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019158
UMLS CUI [2]
C0023890
hiv-positive
Descripción

hiv-positive

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019682
patient is pregnant
Descripción

patient is pregnant

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
patient or guardian is not able to sign informed consent.
Descripción

patient or guardian is not able to sign informed consent.

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Volver a la parte superior de la página

Similar models

Eligibility Acute Myeloid Leukemia NCT00988013

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
patients with the following diseases:
Item
patients with the following diseases: acute myeloid or lymphoblastic leukemia in first complete remission if poor prognosis documented by failure to response after initial induction chemotherapy, or cytogenetic, or molecular studies. acute leukemia in greater/equal second remission, or partial remission after chemotherapy. high grade non hodgkin's or hodgkin's lymphoma with marrow involvement resistant/ relapsed after second line therapy including high dose chemotherapy and autologous sct. cml in advanced or blastic phase. plasma cell leukemia.
boolean
C0023467 (UMLS CUI [1])
C0023474 (UMLS CUI [2])
C0023449 (UMLS CUI [3])
C0019829 (UMLS CUI [4])
C0024305 (UMLS CUI [5])
C0023484 (UMLS CUI [6])
age
Item
age 18-60 years.
boolean
C0001779 (UMLS CUI [1])
karnofsky
Item
karnofsky performance status of 70
boolean
C0206065 (UMLS CUI [1])
cardiac and pulmonary function
Item
adequate cardiac and pulmonary function. patients with decreased lvef less than/equal to 40% or dlco less than/equal to 50% of predicted will require clearance from cardiology or pulmonary services, respectively, prior to enrollment on this protocol.
boolean
C0428772 (UMLS CUI [1])
C1516251 (UMLS CUI [2])
creatinine or creatinine clearance
Item
serum creatinine less than/equal to 1.5 mg/dl or creatinine clearance greater than/equal to 50 ml/min .
boolean
C0201976 (UMLS CUI [1])
C0373595 (UMLS CUI [2])
bilirubin
Item
serum bilirubin 2.0 mg/dl, sgpt less than/equal to 3 times the upper limit of normal
boolean
C1278039 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
life expectancy is severely limited by concomitant illness.
Item
life expectancy is severely limited by concomitant illness.
boolean
C0023671 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
hepatitis
Item
evidence of chronic active hepatitis or cirrhosis
boolean
C0019158 (UMLS CUI [1])
C0023890 (UMLS CUI [2])
hiv
Item
hiv-positive
boolean
C0019682 (UMLS CUI [1])
pregnancy
Item
patient is pregnant
boolean
C0032961 (UMLS CUI [1])
patient or guardian is not able to sign informed consent.
Item
patient or guardian is not able to sign informed consent.
boolean
C0021430 (UMLS CUI [1])
Volver a la parte superior de la página 

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial