ID

43607

Description

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

Lien

https://clinicaltrials.gov/show/NCT01020175

Mots-clés

  1. 07/12/2015 07/12/2015 -
  2. 18/09/2017 18/09/2017 -
  3. 20/09/2021 20/09/2021 -
Téléchargé le

20 septembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Acute Leukemia NCT01020175

Eligibility Acute Leukemia NCT01020175

Inclusion Criteria
Description

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).
Description

acute myelocytic leukemia

Type de données

boolean

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

age

Type de données

boolean

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

ecog performance status

Type de données

boolean

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

hla-identical sibling donor

Type de données

boolean

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

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

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

serum creatinine

Type de données

boolean

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

left ventricular size and function abnormal

Type de données

boolean

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

dlco

Type de données

boolean

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

bilirubin

Type de données

boolean

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

splenectomised or splenic irradiation

Type de données

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.
Description

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

Type de données

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.
Description

study subject participation

Type de données

boolean

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

pregnant or lactating

Type de données

boolean

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

known sensitivity to e.coli derived products

Type de données

boolean

Alias
UMLS CUI [1]
C0020517
hiv positive.
Description

hiv positive

Type de données

boolean

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

previously received bm/pbpc transplant

Type de données

boolean

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

Similar models

Eligibility Acute Leukemia NCT01020175

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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