Informatie:
Fout:
ID
12811
Beschrijving
Trial to Assess the Efficacy of a TCR Alfa Beta Depleted Graft in Pediatric Affected by ALL or AML and Receiving an HSCT; ODM derived from: https://clinicaltrials.gov/show/NCT01810120
Link
https://clinicaltrials.gov/show/NCT01810120
Trefwoorden
Versies (1)
- 21-12-15 21-12-15 -
Geüploaded op
21 december 2015
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Acute Lymphoblastic Leukemia NCT01810120
Eligibility Acute Lymphoblastic Leukemia NCT01810120
- StudyEvent: Eligibility
Similar models
Eligibility Acute Lymphoblastic Leukemia NCT01810120
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
age
Item
patients aged ≥ 3 months and < 21 years
boolean
C0001779 (UMLS CUI [1])
eligible for allogeneic stem cell transplant lacking stem cell donor
Item
patients diagnosed with malignant hemopathies (acute lymphoblastic leukemia (all), acute myeloid leukemia (aml), non-hodgkin lymphoma (nhl)) in complete morphological remission or myelodysplastic syndromes (mds), solid tumors or non malignant hematological disorders (scid, acquired and congenital aplastic anemia, other primary immunodeficiencies, life-threatening cytopenia) eligible for an allogeneic transplantation and lacking a related or unrelated hla-matched donor
boolean
C0013893 (UMLS CUI [1])
C1456094 (UMLS CUI [2])
C0375877 (UMLS CUI [3])
C1456094 (UMLS CUI [2])
C0375877 (UMLS CUI [3])
patients displaying an hla-partially matched family donor
Item
patients displaying an hla-partially matched family donor
boolean
C0375877 (UMLS CUI [1])
lansky/karnofsky score > 40, who > 4
Item
lansky/karnofsky score > 40, who > 4
boolean
C0206065 (UMLS CUI [1])
C1298650 (UMLS CUI [2])
C1298650 (UMLS CUI [2])
informed consent
Item
signed written informed consent
boolean
C0021430 (UMLS CUI [1])
graft versus host disease
Item
grade >ii acute gvhd or chronic extensive gvhd at the time of inclusion
boolean
C0018133 (UMLS CUI [1])
immunosuppressive treatment for gvhd treatment
Item
patient receiving an immunosuppressive treatment for gvhd treatment at the time of inclusion
boolean
C0021079 (UMLS CUI [1])
C0278845 (UMLS CUI [2])
C0278845 (UMLS CUI [2])
renal dysfunction or dysfunction of liver
Item
dysfunction of liver (alt/ast > 5 times normal value, or bilirubin > 3 times normal value), or of renal function (creatinine clearance < 30 ml / min)
boolean
C0086565 (UMLS CUI [1])
C3279454 (UMLS CUI [2])
C3279454 (UMLS CUI [2])
cardiovascular disease
Item
severe cardiovascular disease (arrhythmias requiring chronic treatment, congestive heart failure or left ventricular ejection fraction <40percent)
boolean
C0007222 (UMLS CUI [1])
infection
Item
current active infectious disease (including positive hiv serology or viral rna)
boolean
C0009450 (UMLS CUI [1])
Comorbidity
Item
serious concurrent uncontrolled medical disorder
boolean
C0009488 (UMLS CUI [1])
pregnant or breastfeeding
Item
pregnant or breast feeding female patient
boolean
C0549206 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
informed consent
Item
lack of parents' informed consent.
boolean
C0021430 (UMLS CUI [1])