ID

14458

Descripción

German Multicenter Trial for Treatment of Elderly Patients With Newly Diagnosed Acute Lymphoblastic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00198978

Link

https://clinicaltrials.gov/show/NCT00198978

Palabras clave

  1. 16/4/16 16/4/16 -
Subido en

16 de abril de 2016

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Adult Acute Lymphocytic Leukemia NCT00198978

Eligibility Adult Acute Lymphocytic Leukemia NCT00198978

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of acute lymphoblastic leukemia (pro b, pre b, c-all or t-all), proved by morphology and immunophenotyping
Descripción

Acute lymphocytic leukemia

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023449
age > 55 yrs (no upper age limit)
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
written informed consent
Descripción

written informed consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe leukemia associated complications, not controllable before therapy onset e.g.
Descripción

cancer complication

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0596237
life threatening infections as sepsis, pneumonia, hypoxia, shock, life threatening bleeding)
Descripción

Communicable Diseases

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009450
decompensated renal failure if not caused by leukemia with creatinine > 2x uln
Descripción

Kidney Failure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0035078
heart failure (nyha ii/iv), instable angina, significant coronary stenosis
Descripción

Heart failure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018801
hepatic insufficiency e.g. liver cirrhosis or chronic active hepatitis with bilirubin > 1,5 x uln and/or asa, ala, ap > 2,5 uln
Descripción

Hepatic Insufficiency

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1306571
decompensated metabolic disturbances (e.g. not controllable diabetes)
Descripción

metabolic disturbance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0746556
severe obstructive or restrictive pulmonary disease with hypoxaemia
Descripción

Chronic Obstructive Airway Disease or Restrictive pulmonary disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0024117
UMLS CUI [2]
C0877013
severe psychiatric illness or other circumstances which may compromise cooperation of the patient
Descripción

Mental disorders

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004936
active second neoplasia
Descripción

Second Primary Neoplasms

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0085183
hiv infection
Descripción

HIV Infection

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019693
severely reduced general condition
Descripción

Reduced general condition

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1112627
cytostatic pre-treatment of all
Descripción

Cytostatic chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2609342
chemotherapy treatment of any other malignancy during the last 5 years
Descripción

Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3665472
participation in other clinical trials interfering with the study therapy
Descripción

participation in other clinical trials

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Adult Acute Lymphocytic Leukemia NCT00198978

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Acute lymphocytic leukemia
Item
diagnosis of acute lymphoblastic leukemia (pro b, pre b, c-all or t-all), proved by morphology and immunophenotyping
boolean
C0023449 (UMLS CUI [1])
Age
Item
age > 55 yrs (no upper age limit)
boolean
C0001779 (UMLS CUI [1])
written informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
cancer complication
Item
severe leukemia associated complications, not controllable before therapy onset e.g.
boolean
C0596237 (UMLS CUI [1])
Communicable Diseases
Item
life threatening infections as sepsis, pneumonia, hypoxia, shock, life threatening bleeding)
boolean
C0009450 (UMLS CUI [1])
Kidney Failure
Item
decompensated renal failure if not caused by leukemia with creatinine > 2x uln
boolean
C0035078 (UMLS CUI [1])
Heart failure
Item
heart failure (nyha ii/iv), instable angina, significant coronary stenosis
boolean
C0018801 (UMLS CUI [1])
Hepatic Insufficiency
Item
hepatic insufficiency e.g. liver cirrhosis or chronic active hepatitis with bilirubin > 1,5 x uln and/or asa, ala, ap > 2,5 uln
boolean
C1306571 (UMLS CUI [1])
metabolic disturbance
Item
decompensated metabolic disturbances (e.g. not controllable diabetes)
boolean
C0746556 (UMLS CUI [1])
Chronic Obstructive Airway Disease or Restrictive pulmonary disease
Item
severe obstructive or restrictive pulmonary disease with hypoxaemia
boolean
C0024117 (UMLS CUI [1])
C0877013 (UMLS CUI [2])
Mental disorders
Item
severe psychiatric illness or other circumstances which may compromise cooperation of the patient
boolean
C0004936 (UMLS CUI [1])
Second Primary Neoplasms
Item
active second neoplasia
boolean
C0085183 (UMLS CUI [1])
HIV Infection
Item
hiv infection
boolean
C0019693 (UMLS CUI [1])
Reduced general condition
Item
severely reduced general condition
boolean
C1112627 (UMLS CUI [1])
Cytostatic chemotherapy
Item
cytostatic pre-treatment of all
boolean
C2609342 (UMLS CUI [1])
Chemotherapy
Item
chemotherapy treatment of any other malignancy during the last 5 years
boolean
C3665472 (UMLS CUI [1])
participation in other clinical trials
Item
participation in other clinical trials interfering with the study therapy
boolean
C2348568 (UMLS CUI [1])

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