ID

13053

Descrizione

Rituxan and BEAM With Autologous Peripheral Blood Progenitor Transplant for Indolent Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00572013

collegamento

https://clinicaltrials.gov/show/NCT00572013

Keywords

  1. 13/01/16 13/01/16 -
Titolare del copyright

CC BY-NC 3.0

Caricato su

13 gennaio 2016

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

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Eligibility Lymphoma NCT00572013

Eligibility Lymphoma NCT00572013

  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00572013
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
any low-grade b-cell, cd20 positive, non-hodgkin's lymphoma that is felt to otherwise be a transplant candidate (relapsed, induction failure, first pr or cr). specifically: small lymphocytic, marginal zone, mantle cell, and follicular histologies.
Descrizione

non-hodgkin's lymphoma

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0024305
at least 19 years of age
Descrizione

age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
signed written informed consent
Descrizione

informed consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
expected survival of at least 6 months
Descrizione

life expectancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0023671
subjects with out history of t-cell lymphoma
Descrizione

t-cell lymphoma

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0079772
who performance status greater or equal to 2
Descrizione

who performance status

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1298650
subjects without serious disease or condition that, in the opinion of the investigator, would compromise the subject's ability to participate in the study.
Descrizione

subjects without serious disease or condition that, in the opinion of the investigator, would compromise the subject's ability to participate in the study

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
non-pregnant and non-lactating women
Descrizione

pregnancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
male or female subjects of reproductive potential who are able to follow accepted birth control measures.
Descrizione

contraception

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0700589

Similar models

Eligibility Lymphoma NCT00572013

  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00572013
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
non-hodgkin's lymphoma
Item
any low-grade b-cell, cd20 positive, non-hodgkin's lymphoma that is felt to otherwise be a transplant candidate (relapsed, induction failure, first pr or cr). specifically: small lymphocytic, marginal zone, mantle cell, and follicular histologies.
boolean
C0024305 (UMLS CUI [1])
age
Item
at least 19 years of age
boolean
C0001779 (UMLS CUI [1])
informed consent
Item
signed written informed consent
boolean
C0021430 (UMLS CUI [1])
life expectancy
Item
expected survival of at least 6 months
boolean
C0023671 (UMLS CUI [1])
t-cell lymphoma
Item
subjects with out history of t-cell lymphoma
boolean
C0079772 (UMLS CUI [1])
who performance status
Item
who performance status greater or equal to 2
boolean
C1298650 (UMLS CUI [1])
subjects without serious disease or condition that, in the opinion of the investigator, would compromise the subject's ability to participate in the study
Item
subjects without serious disease or condition that, in the opinion of the investigator, would compromise the subject's ability to participate in the study.
boolean
C2348563 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
pregnancy
Item
non-pregnant and non-lactating women
boolean
C0032961 (UMLS CUI [1])
contraception
Item
male or female subjects of reproductive potential who are able to follow accepted birth control measures.
boolean
C0700589 (UMLS CUI [1])

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