ID

13141

Beskrivning

Donor-specific Allogeneic Hematopoietic Cell Transplantation for Acute Lymphoblastic Leukemia (ALL); ODM derived from: https://clinicaltrials.gov/show/NCT01037764

Länk

https://clinicaltrials.gov/show/NCT01037764

Nyckelord

  1. 2016-01-19 2016-01-19 -
Rättsinnehavare

CC BY-NC 3.0

Uppladdad den

19 januari 2016

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Acute Lymphoid Leukemia NCT01037764

Eligibility Acute Lymphoid Leukemia NCT01037764

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with all who achieve cr after induction chemotherapy.
Beskrivning

patients with all who achieve cr after induction chemotherapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0023449
patients with recurrent all that went into second cr after salvage chemotherapy, except those who had undergone allogeneic hct previously.
Beskrivning

recurrent all that went into second cr after salvage chemotherapy, except those who had undergone allogeneic hct previously

Datatyp

boolean

Alias
UMLS CUI [1]
C0023449
patients should be 15 years of age or more, and 75 years of age or less.
Beskrivning

age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
the performance status of the patients should be 70 or over by karnofsky performance scale.
Beskrivning

karnofsky performance status

Datatyp

boolean

Alias
UMLS CUI [1]
C0206065
patients should have adequate hepatic function (bilirubin less than 2.0 mg/dl, ast less than three times the upper normal limit).
Beskrivning

patients should have adequate hepatic function (bilirubin less than 2.0 mg/dl, ast less than three times the upper normal limit)

Datatyp

boolean

Alias
UMLS CUI [1]
C1278039
UMLS CUI [2]
C0201899
patients must have adequate renal function (creatinine less than 2.0 mg/dl).
Beskrivning

creatinine

Datatyp

boolean

Alias
UMLS CUI [1]
C0201976
patients must have adequate cardiac function (ejection fraction > 40% on muga scan).
Beskrivning

ejection fraction

Datatyp

boolean

Alias
UMLS CUI [1]
C0232174
patients must sign informed consent.
Beskrivning

informed consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
presence of significant active infection
Beskrivning

infection

Datatyp

boolean

Alias
UMLS CUI [1]
C0009450
presence of uncontrolled bleeding
Beskrivning

bleeding

Datatyp

boolean

Alias
UMLS CUI [1]
C0019080
any coexisting major illness or organ failure
Beskrivning

comorbidity

Datatyp

boolean

Alias
UMLS CUI [1]
C0009488
patients with psychiatric disorder or mental deficiency severe as to make compliance with the treatment unlike, and making informed consent impossible
Beskrivning

patients with psychiatric disorder or mental deficiency severe as to make compliance with the treatment unlike, and making informed consent impossible

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
nursing women, pregnant women, women of childbearing potential who do not want adequate contraception
Beskrivning

nursing women, pregnant women, women of childbearing potential who do not want adequate contraception

Datatyp

boolean

Alias
UMLS CUI [1]
C0006147
UMLS CUI [2]
C0032961
UMLS CUI [3]
C0700589
patients with a diagnosis of prior malignancy unless disease-free for at least 5 years following therapy with curative intent (except curatively treated nonmelanoma skin cancer, in situ carcinoma, or cervical intraepithelial neoplasia)
Beskrivning

malignancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0006826

Similar models

Eligibility Acute Lymphoid Leukemia NCT01037764

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
patients with all who achieve cr after induction chemotherapy
Item
patients with all who achieve cr after induction chemotherapy.
boolean
C0023449 (UMLS CUI [1])
recurrent all that went into second cr after salvage chemotherapy, except those who had undergone allogeneic hct previously
Item
patients with recurrent all that went into second cr after salvage chemotherapy, except those who had undergone allogeneic hct previously.
boolean
C0023449 (UMLS CUI [1])
age
Item
patients should be 15 years of age or more, and 75 years of age or less.
boolean
C0001779 (UMLS CUI [1])
karnofsky performance status
Item
the performance status of the patients should be 70 or over by karnofsky performance scale.
boolean
C0206065 (UMLS CUI [1])
patients should have adequate hepatic function (bilirubin less than 2.0 mg/dl, ast less than three times the upper normal limit)
Item
patients should have adequate hepatic function (bilirubin less than 2.0 mg/dl, ast less than three times the upper normal limit).
boolean
C1278039 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
creatinine
Item
patients must have adequate renal function (creatinine less than 2.0 mg/dl).
boolean
C0201976 (UMLS CUI [1])
ejection fraction
Item
patients must have adequate cardiac function (ejection fraction > 40% on muga scan).
boolean
C0232174 (UMLS CUI [1])
informed consent
Item
patients must sign informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
infection
Item
presence of significant active infection
boolean
C0009450 (UMLS CUI [1])
bleeding
Item
presence of uncontrolled bleeding
boolean
C0019080 (UMLS CUI [1])
comorbidity
Item
any coexisting major illness or organ failure
boolean
C0009488 (UMLS CUI [1])
patients with psychiatric disorder or mental deficiency severe as to make compliance with the treatment unlike, and making informed consent impossible
Item
patients with psychiatric disorder or mental deficiency severe as to make compliance with the treatment unlike, and making informed consent impossible
boolean
C0021430 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
nursing women, pregnant women, women of childbearing potential who do not want adequate contraception
Item
nursing women, pregnant women, women of childbearing potential who do not want adequate contraception
boolean
C0006147 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
C0700589 (UMLS CUI [3])
malignancy
Item
patients with a diagnosis of prior malignancy unless disease-free for at least 5 years following therapy with curative intent (except curatively treated nonmelanoma skin cancer, in situ carcinoma, or cervical intraepithelial neoplasia)
boolean
C0006826 (UMLS CUI [1])

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