Informationen:
Fehler:
ID
41081
Beschreibung
Study to Predict Risk of Relapse in Bone Marrow Cell Samples From Younger Patients With Acute Myeloid Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT01438138
Link
https://clinicaltrials.gov/show/NCT01438138
Stichworte
Versionen (1)
- 21.06.20 21.06.20 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
21. Juni 2020
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Leukemia NCT01438138
Eligibility Leukemia NCT01438138
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Leukemia NCT01438138
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Leukemia, Myelocytic, Acute | Exception Acute Promyelocytic Leukemia
Item
patients with confirmed non-m3 acute myeloid leukemia
boolean
C0023467 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0023487 (UMLS CUI [2,2])
C1705847 (UMLS CUI [2,1])
C0023487 (UMLS CUI [2,2])
Therapy Treatment Protocols Specified
Item
treated on cog-aaml03p1 or cog- aaml0531 protocols
boolean
C0087111 (UMLS CUI [1,1])
C0040808 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
C0040808 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Sample Treatment Protocol Specified
Item
samples from cog-aaml0531 can come from either treatment arm, but these samples need to be independent from any patients who donated samples assayed in study cog-aaml11b2
boolean
C0370003 (UMLS CUI [1,1])
C0040808 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
C0040808 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Exclusion Down Syndrome
Item
patients with down syndrome are excluded
boolean
C0680251 (UMLS CUI [1,1])
C0013080 (UMLS CUI [1,2])
C0013080 (UMLS CUI [1,2])
Bone Marrow mononuclear cells | Specimen Cryopreserved
Item
cryopreserved bone marrow mononuclear cell (bmmc) samples collected at diagnosis, prior to start induction therapy
boolean
C0005953 (UMLS CUI [1,1])
C0806987 (UMLS CUI [1,2])
C0370003 (UMLS CUI [2,1])
C0010405 (UMLS CUI [2,2])
C0806987 (UMLS CUI [1,2])
C0370003 (UMLS CUI [2,1])
C0010405 (UMLS CUI [2,2])
Specimen Cryopreserved Clinical Study Site
Item
samples must have been cryopreserved at central lab within 3 days of draw at clinical site
boolean
C0370003 (UMLS CUI [1,1])
C0010405 (UMLS CUI [1,2])
C2347790 (UMLS CUI [1,3])
C0010405 (UMLS CUI [1,2])
C2347790 (UMLS CUI [1,3])
Target Amount Cells Frozen
Item
target of 10 x 10^6 cells frozen
boolean
C1521840 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0007634 (UMLS CUI [1,3])
C0016701 (UMLS CUI [1,4])
C1265611 (UMLS CUI [1,2])
C0007634 (UMLS CUI [1,3])
C0016701 (UMLS CUI [1,4])
Annotation Clinical Required
Item
patients' clinical annotations required after unblinding
boolean
C1706814 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C1514873 (UMLS CUI [1,3])
C0205210 (UMLS CUI [1,2])
C1514873 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])
Prior Therapy Concurrent
Item
prior concurrent therapy:
boolean
C1514463 (UMLS CUI [1,1])
C0205420 (UMLS CUI [1,2])
C0205420 (UMLS CUI [1,2])
ID.12
Item
see disease characteristics
boolean