ID

13277

Beschrijving

Radiolabeled BC8 Antibody, Busulfan, Cyclophosphamide Followed by Donor Stem Cell Transplant in Treating Patients With Acute Myelogenous Leukemia in First Remission; ODM derived from: https://clinicaltrials.gov/show/NCT00005940

Link

https://clinicaltrials.gov/show/NCT00005940

Trefwoorden

Versies (1)
  1. 29-01-16 29-01-16 -
Geüploaded op

29 januari 2016

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Adult Acute Myeloid Leukemia in Remission NCT00005940

Engels

Eligibility Adult Acute Myeloid Leukemia in Remission NCT00005940

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with aml in first remission
Beschrijving

AML

Datatype

boolean

Alias
UMLS CUI [1]
C0153886
creatinine < 2.0 mg/dl
Beschrijving

renal function

Datatype

boolean

Alias
UMLS CUI [1]
C0201976
bilirubin < 1.5 mg/dl which is expected to exclude patients at high risk of developing veno-occlusive disease of the liver
Beschrijving

Liver function

Datatype

boolean

Alias
UMLS CUI [1]
C1278039
aspartate aminotransferase (ast) < 1.5 times the upper limit of normal which is expected to exclude patients at high risk of developing veno-occlusive disease of the liver
Beschrijving

Liver function

Datatype

boolean

Alias
UMLS CUI [1]
C0201899
patients must have an expected survival of > 60 days and must be free of major infection
Beschrijving

Life expectancy and infections

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
UMLS CUI [2]
C0009450
donor: genotypic or phenotypic hla-matched family members; related donors should be matched by molecular methods at the intermediate resolution level at hla-a, b, c, and dr beta 1 (drb1) according to fred hutchinson cancer research center (fhcrc) standard practice guidelines and to the allele level at dq beta 1 (dqb1)
Beschrijving

Donor criteria

Datatype

boolean

Alias
UMLS CUI [1,1]
C0301618
UMLS CUI [1,2]
C2327792
UMLS CUI [1,3]
C0086282
UMLS CUI [2,1]
C0031437
UMLS CUI [2,2]
C2327792
UMLS CUI [2,3]
C0086282
UMLS CUI [3]
C0019728
UMLS CUI [4]
C0019737
UMLS CUI [5]
C0019751
UMLS CUI [6]
C0122040
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with history of or current leukemic involvement of the central nervous system (cns)
Beschrijving

leukemic involvement of the central nervous system

Datatype

boolean

Alias
UMLS CUI [1]
C1332884
prior radiation to maximally tolerated levels to any normal organ
Beschrijving

Radiation

Datatype

boolean

Alias
UMLS CUI [1]
C0851346
inability to understand or give an informed consent
Beschrijving

Informed consent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
patients who are seropositive for human immunodeficiency virus (hiv)
Beschrijving

HIV

Datatype

boolean

Alias
UMLS CUI [1]
C0019699
perceived inability to tolerate diagnostic or therapeutic procedures, particularly treatment in radiation isolation
Beschrijving

Compliance

Datatype

boolean

Alias
UMLS CUI [1,1]
C0851346
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C1321605
circulating antibody against mouse immunoglobulin
Beschrijving

Human anti-mouse antibody

Datatype

boolean

Alias
UMLS CUI [1]
C1295018
donor: unrelated donors and donors mismatched for 1 or more hla antigens
Beschrijving

donor exclusion criteria

Datatype

boolean

Alias
UMLS CUI [1]
C0086282
UMLS CUI [2,1]
C0854634
UMLS CUI [2,2]
C0019721
donor: donors who for psychologic, physiologic or medical reasons are unable to undergo filgrastim (g-csf)- mobilized pbsc collection or marrow harvesting
Beschrijving

Donor exclusion criteria

Datatype

boolean

Alias
UMLS CUI [1,1]
C0439801
UMLS CUI [1,2]
C1321605
UMLS CUI [1,3]
C0210630
UMLS CUI [2,1]
C0439801
UMLS CUI [2,2]
C1321605
UMLS CUI [2,3]
C3702379
donor: donors who are seropositive for hiv
Beschrijving

Donor exclusion criteria

Datatype

boolean

Alias
UMLS CUI [1]
C0019699
Terug naar het begin van de pagina

Similar models

Eligibility Adult Acute Myeloid Leukemia in Remission NCT00005940

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
AML
Item
patients with aml in first remission
boolean
C0153886 (UMLS CUI [1])
renal function
Item
creatinine < 2.0 mg/dl
boolean
C0201976 (UMLS CUI [1])
Liver function
Item
bilirubin < 1.5 mg/dl which is expected to exclude patients at high risk of developing veno-occlusive disease of the liver
boolean
C1278039 (UMLS CUI [1])
Liver function
Item
aspartate aminotransferase (ast) < 1.5 times the upper limit of normal which is expected to exclude patients at high risk of developing veno-occlusive disease of the liver
boolean
C0201899 (UMLS CUI [1])
Life expectancy and infections
Item
patients must have an expected survival of > 60 days and must be free of major infection
boolean
C0023671 (UMLS CUI [1])
C0009450 (UMLS CUI [2])
Donor criteria
Item
donor: genotypic or phenotypic hla-matched family members; related donors should be matched by molecular methods at the intermediate resolution level at hla-a, b, c, and dr beta 1 (drb1) according to fred hutchinson cancer research center (fhcrc) standard practice guidelines and to the allele level at dq beta 1 (dqb1)
boolean
C0301618 (UMLS CUI [1,1])
C2327792 (UMLS CUI [1,2])
C0086282 (UMLS CUI [1,3])
C0031437 (UMLS CUI [2,1])
C2327792 (UMLS CUI [2,2])
C0086282 (UMLS CUI [2,3])
C0019728 (UMLS CUI [3])
C0019737 (UMLS CUI [4])
C0019751 (UMLS CUI [5])
C0122040 (UMLS CUI [6])
Item Group
C0680251 (UMLS CUI)
leukemic involvement of the central nervous system
Item
patients with history of or current leukemic involvement of the central nervous system (cns)
boolean
C1332884 (UMLS CUI [1])
Radiation
Item
prior radiation to maximally tolerated levels to any normal organ
boolean
C0851346 (UMLS CUI [1])
Informed consent
Item
inability to understand or give an informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
HIV
Item
patients who are seropositive for human immunodeficiency virus (hiv)
boolean
C0019699 (UMLS CUI [1])
Compliance
Item
perceived inability to tolerate diagnostic or therapeutic procedures, particularly treatment in radiation isolation
boolean
C0851346 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C1321605 (UMLS CUI [1,3])
Human anti-mouse antibody
Item
circulating antibody against mouse immunoglobulin
boolean
C1295018 (UMLS CUI [1])
donor exclusion criteria
Item
donor: unrelated donors and donors mismatched for 1 or more hla antigens
boolean
C0086282 (UMLS CUI [1])
C0854634 (UMLS CUI [2,1])
C0019721 (UMLS CUI [2,2])
Donor exclusion criteria
Item
donor: donors who for psychologic, physiologic or medical reasons are unable to undergo filgrastim (g-csf)- mobilized pbsc collection or marrow harvesting
boolean
C0439801 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
C0210630 (UMLS CUI [1,3])
C0439801 (UMLS CUI [2,1])
C1321605 (UMLS CUI [2,2])
C3702379 (UMLS CUI [2,3])
Donor exclusion criteria
Item
donor: donors who are seropositive for hiv
boolean
C0019699 (UMLS CUI [1])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial