Information:
Error:
ID
13141
Description
Donor-specific Allogeneic Hematopoietic Cell Transplantation for Acute Lymphoblastic Leukemia (ALL); ODM derived from: https://clinicaltrials.gov/show/NCT01037764
Link
https://clinicaltrials.gov/show/NCT01037764
Keywords
Versions (1)
- 1/19/16 1/19/16 -
Copyright Holder
CC BY-NC 3.0
Uploaded on
January 19, 2016
DOI
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License
Creative Commons BY-NC 3.0
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Eligibility Acute Lymphoid Leukemia NCT01037764
Eligibility Acute Lymphoid Leukemia NCT01037764
- StudyEvent: Eligibility
Similar models
Eligibility Acute Lymphoid Leukemia NCT01037764
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
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])
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])
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])
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])
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])