ID

13727

Description

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

Keywords

  1. 3/1/16 3/1/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

March 1, 2016

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Acute Myeloid Leukemia NCT00988013

Eligibility Acute Myeloid Leukemia NCT00988013

Inclusion Criteria
Description

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.
Description

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.

Data type

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.
Description

age 18-60 years.

Data type

boolean

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

karnofsky performance status of 70

Data type

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.
Description

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.

Data type

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 .
Description

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

Data type

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
Description

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

Data type

boolean

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

Exclusion Criteria

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

life expectancy is severely limited by concomitant illness.

Data type

boolean

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

evidence of chronic active hepatitis or cirrhosis

Data type

boolean

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

hiv-positive

Data type

boolean

Alias
UMLS CUI [1]
C0019682
patient is pregnant
Description

patient is pregnant

Data type

boolean

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

patient or guardian is not able to sign informed consent.

Data type

boolean

Alias
UMLS CUI [1]
C0021430

Similar models

Eligibility Acute Myeloid Leukemia NCT00988013

Name
Type
Description | Question | Decode (Coded Value)
Data type
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])

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

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