ID

43607

Descrizione

Peripheral Blood (PB) Versus Bone Marrow (BM) in Allogeneic Stem Cell Transplantation; ODM derived from: https://clinicaltrials.gov/show/NCT01020175

collegamento

https://clinicaltrials.gov/show/NCT01020175

Keywords

  1. 07/12/15 07/12/15 -
  2. 18/09/17 18/09/17 -
  3. 20/09/21 20/09/21 -
Caricato su

20 settembre 2021

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Eligibility Acute Leukemia NCT01020175

Eligibility Acute Leukemia NCT01020175

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with either diagnosis of aml in first or second remission, in first untreated relapse (blast count in marrow < 30 percent); all in first or second remission, in first untreated relapse (blast count in marrow < 30 percent); cml in first chronic phase, in first accelerated phase (total blast and promyelocytes in marrow and or peripheral blood < 30 percent) or mds (excluding raeb-t).
Descrizione

acute myelocytic leukemia

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0023467
age between 18 and 55 years.
Descrizione

age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
ecog performance status between 0,1 or 2.
Descrizione

ecog performance status

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1520224
hla-identical sibling donor.
Descrizione

hla-identical sibling donor

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0019633
UMLS CUI [2]
C1960320
written informed consent.
Descrizione

informed consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
serum creatinine more than 10 percent above the normal range for the centre.
Descrizione

serum creatinine

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0700225
left ventricular size and function abnormal.
Descrizione

left ventricular size and function abnormal

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2073541
UMLS CUI [2]
C0242698
dlco < 50 percent.
Descrizione

dlco

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1516251
bilirubin > 2mg/dl (34.2 µmol/l).
Descrizione

bilirubin

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1278039
splenectomised or splenic irradiation.
Descrizione

splenectomised or splenic irradiation

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0037995
psychiatric, addictive, or any other disorder, which compromises ability to give truly informed consent for participation in this study.
Descrizione

psychiatric, addictive, or any other disorder, which compromises ability to give truly informed consent for participation in this study

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
currently receiving non-licensed drugs which may affect gvhd or engraftment.
Descrizione

study subject participation

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2348568
pregnant or lactating women.
Descrizione

pregnant or lactating

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0549206
UMLS CUI [2]
C2828358
known sensitivity to e.coli derived products.
Descrizione

known sensitivity to e.coli derived products

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0020517
hiv positive.
Descrizione

hiv positive

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0019699
previously received bm/pbpc transplant.
Descrizione

previously received bm/pbpc transplant

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0005961
UMLS CUI [2]
C0242602

Similar models

Eligibility Acute Leukemia NCT01020175

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
acute myelocytic leukemia
Item
patients with either diagnosis of aml in first or second remission, in first untreated relapse (blast count in marrow < 30 percent); all in first or second remission, in first untreated relapse (blast count in marrow < 30 percent); cml in first chronic phase, in first accelerated phase (total blast and promyelocytes in marrow and or peripheral blood < 30 percent) or mds (excluding raeb-t).
boolean
C0023467 (UMLS CUI [1])
age
Item
age between 18 and 55 years.
boolean
C0001779 (UMLS CUI [1])
ecog performance status
Item
ecog performance status between 0,1 or 2.
boolean
C1520224 (UMLS CUI [1])
hla-identical sibling donor
Item
hla-identical sibling donor.
boolean
C0019633 (UMLS CUI [1])
C1960320 (UMLS CUI [2])
informed consent
Item
written informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
serum creatinine
Item
serum creatinine more than 10 percent above the normal range for the centre.
boolean
C0700225 (UMLS CUI [1])
left ventricular size and function abnormal
Item
left ventricular size and function abnormal.
boolean
C2073541 (UMLS CUI [1])
C0242698 (UMLS CUI [2])
dlco
Item
dlco < 50 percent.
boolean
C1516251 (UMLS CUI [1])
bilirubin
Item
bilirubin > 2mg/dl (34.2 µmol/l).
boolean
C1278039 (UMLS CUI [1])
splenectomised or splenic irradiation
Item
splenectomised or splenic irradiation.
boolean
C0037995 (UMLS CUI [1])
psychiatric, addictive, or any other disorder, which compromises ability to give truly informed consent for participation in this study
Item
psychiatric, addictive, or any other disorder, which compromises ability to give truly informed consent for participation in this study.
boolean
C0021430 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
study subject participation
Item
currently receiving non-licensed drugs which may affect gvhd or engraftment.
boolean
C2348568 (UMLS CUI [1])
pregnant or lactating
Item
pregnant or lactating women.
boolean
C0549206 (UMLS CUI [1])
C2828358 (UMLS CUI [2])
known sensitivity to e.coli derived products
Item
known sensitivity to e.coli derived products.
boolean
C0020517 (UMLS CUI [1])
hiv positive
Item
hiv positive.
boolean
C0019699 (UMLS CUI [1])
previously received bm/pbpc transplant
Item
previously received bm/pbpc transplant.
boolean
C0005961 (UMLS CUI [1])
C0242602 (UMLS CUI [2])

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