ID

13812

Descrição

A Phase I Study of OCV-501 in Acute Myeloid Leukemia Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01440920

Link

https://clinicaltrials.gov/show/NCT01440920

Palavras-chave

  1. 07/03/2016 07/03/2016 -
  2. 07/03/2016 07/03/2016 -
Transferido a

7 de março de 2016

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Acute Myeloid Leukemia NCT01440920

Eligibility Acute Myeloid Leukemia NCT01440920

Criteria
Descrição

Criteria

Alias
UMLS CUI-1
C1512693
patients with acute myeloid leukemia including patients with secondary leukemia. however, the patients with mds apparently evolved itno aml and patients with aml accompanied by t(15;17)(q22;q12),(pml/raralpha) , should be excluded.
Descrição

AML

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0023467
UMLS CUI [2]
C2825139
UMLS CUI [3]
C0280449
patients who achieved the first complete remission after the induction regimen and finished a standard consolidation therapy.
Descrição

complete remission after induction regmin and standard consolidation

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0677874
UMLS CUI [2]
C0392920
age: ≥ 60years of age(at the time of signature of the informed consent form)
Descrição

age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
sex: male and female
Descrição

gender

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0079399
patients who are capable of giving informed consent
Descrição

informed consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
patient's blasts cells show expression of wt1mrna, detected by quantitative rt-pcr.
Descrição

WT1

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0694898
UMLS CUI [2]
C0368761
patients must be one of the following hla drb1 types: hla-drb1*01:01, *04:05, *15:01, *15:02, *08:03 and *09:01.
Descrição

HLA drb1

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0122040
Exclusion criteria
Descrição

Exclusion criteria

Alias
UMLS CUI-1
C0680251
patients who are scheduled for a bone marrow transplantation
Descrição

bone marrow transplantation

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0005961
UMLS CUI [1,2]
C1301732
patients who were administered exceeded acceptable therapeutic dose of immunosuppressants and adrenal cortical steroids.
Descrição

immunosuppressant and steroids

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021081
UMLS CUI [2]
C0038317
patients with uncontrollable active infectious diseases
Descrição

infection

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0009450
patients with autoimmune diseases (including hashimoto's disease, idiopathic thrombocytopenic purpura, and autoimmune hepatitis) or with a medical history of active autoimmune diseases
Descrição

autoimmune diseases

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0004364
immunocompetent patients
Descrição

immunocompetent patients

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1512656
patients with a complication of interstitial pneumonia or with a medical history of interstitial pneumonia
Descrição

interstitial pneumonia

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0206061

Similar models

Eligibility Acute Myeloid Leukemia NCT01440920

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Criteria
C1512693 (UMLS CUI-1)
AML
Item
patients with acute myeloid leukemia including patients with secondary leukemia. however, the patients with mds apparently evolved itno aml and patients with aml accompanied by t(15;17)(q22;q12),(pml/raralpha) , should be excluded.
boolean
C0023467 (UMLS CUI [1])
C2825139 (UMLS CUI [2])
C0280449 (UMLS CUI [3])
complete remission after induction regmin and standard consolidation
Item
patients who achieved the first complete remission after the induction regimen and finished a standard consolidation therapy.
boolean
C0677874 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
age
Item
age: ≥ 60years of age(at the time of signature of the informed consent form)
boolean
C0001779 (UMLS CUI [1])
gender
Item
sex: male and female
boolean
C0079399 (UMLS CUI [1])
informed consent
Item
patients who are capable of giving informed consent
boolean
C0021430 (UMLS CUI [1])
WT1
Item
patient's blasts cells show expression of wt1mrna, detected by quantitative rt-pcr.
boolean
C0694898 (UMLS CUI [1])
C0368761 (UMLS CUI [2])
HLA drb1
Item
patients must be one of the following hla drb1 types: hla-drb1*01:01, *04:05, *15:01, *15:02, *08:03 and *09:01.
boolean
C0122040 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI-1)
bone marrow transplantation
Item
patients who are scheduled for a bone marrow transplantation
boolean
C0005961 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
immunosuppressant and steroids
Item
patients who were administered exceeded acceptable therapeutic dose of immunosuppressants and adrenal cortical steroids.
boolean
C0021081 (UMLS CUI [1])
C0038317 (UMLS CUI [2])
infection
Item
patients with uncontrollable active infectious diseases
boolean
C0009450 (UMLS CUI [1])
autoimmune diseases
Item
patients with autoimmune diseases (including hashimoto's disease, idiopathic thrombocytopenic purpura, and autoimmune hepatitis) or with a medical history of active autoimmune diseases
boolean
C0004364 (UMLS CUI [1])
immunocompetent patients
Item
immunocompetent patients
boolean
C1512656 (UMLS CUI [1])
interstitial pneumonia
Item
patients with a complication of interstitial pneumonia or with a medical history of interstitial pneumonia
boolean
C0206061 (UMLS CUI [1])

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