ID

30232

Descrizione

A Study of Enzastaurin in Patients With Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00452257

collegamento

https://clinicaltrials.gov/show/NCT00452257

Keywords

versioni (1)
  1. 23/05/18 23/05/18 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

23 maggio 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Leukemia, Lymphocytic NCT00452257

Inglese

Eligibility Leukemia, Lymphocytic NCT00452257

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients are eligible to be included in the study only if they meet all of the following criteria:
Descrizione

Criteria Fulfill

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
1. patients with b-cell cll as diagnosed by expression of cd19, cd5, and cd23 by flow cytometry.
Descrizione

Chronic Lymphocytic Leukemia | CD19 Expressing Cell Count Flow Cytometry | CD5 Expressing Cell Measurement Flow Cytometry | CD23 Antigen Flow Cytometry

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0023434
UMLS CUI [2,1]
C3540683
UMLS CUI [2,2]
C0016263
UMLS CUI [3,1]
C3538992
UMLS CUI [3,2]
C0016263
UMLS CUI [4,1]
C0123242
UMLS CUI [4,2]
C0016263
2. rai stage iii or iv disease or earlier stage disease with indications for therapy per nci working group criteria (cheson et al. 1996)
Descrizione

Disease Rai Staging System | Indication Therapeutic procedure

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C1514715
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C0087111
3. absolute lymphocyte count > or = to 5,000/microliter, with a lymphocyte wbc differential of > or = to 70%.
Descrizione

Absolute lymphocyte count | Determination of percentage differential white blood cells

Tipo di dati

boolean

Alias
UMLS CUI [1]
C3544087
UMLS CUI [2]
C0579194
4. platelet count >20,000/microliter.
Descrizione

Platelet Count measurement

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032181
5. adequate organ function, including the following:
Descrizione

Organ function

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0678852
hepatic: bilirubin < or = to 1.5 times the upper limit of normal (x uln); alkaline phosphatase (alp), aspartate transaminase (ast), and alanine transaminase (alt) < or = to 2.5 x uln
Descrizione

Liver function | Serum total bilirubin measurement | Alkaline phosphatase measurement | Aspartate aminotransferase measurement | Alanine aminotransferase measurement

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0232741
UMLS CUI [2]
C1278039
UMLS CUI [3]
C0201850
UMLS CUI [4]
C0201899
UMLS CUI [5]
C0201836
renal: serum creatinine < or = to 1.5 x uln.
Descrizione

Renal function | Creatinine measurement, serum

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0232804
UMLS CUI [2]
C0201976
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients will be excluded from the study if they meet any of the following criteria:
Descrizione

Criteria Fulfill

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
1. are unable to swallow tablets.
Descrizione

Lacking Able to swallow Tablets

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C2712086
UMLS CUI [1,3]
C0039225
2. are unable to discontinue use of carbamazepine, phenobarbital, and phenytoin.
Descrizione

Carbamazepine Discontinue Unable | Phenobarbital Discontinue Unable | Phenytoin Discontinue Unable

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0006949
UMLS CUI [1,2]
C1444662
UMLS CUI [1,3]
C1299582
UMLS CUI [2,1]
C0031412
UMLS CUI [2,2]
C1444662
UMLS CUI [2,3]
C1299582
UMLS CUI [3,1]
C0031507
UMLS CUI [3,2]
C1444662
UMLS CUI [3,3]
C1299582
3. are pregnant or breastfeeding.
Descrizione

Pregnancy | Breast Feeding

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
4. have central nervous system (cns) metastases (unless the patient has completed successful local therapy for cns metastases and has been off of corticosteroids for at least 4 weeks before starting study therapy).
Descrizione

CNS metastases | Exception Local Therapy Completed | Exception Adrenal Cortex Hormones Discontinued

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0686377
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C1517925
UMLS CUI [2,3]
C0205197
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0001617
UMLS CUI [3,3]
C1444662
5. have a serious concomitant systemic disorder (including active bacterial, fungal, or viral infection) that, in the opinion of the investigator, would compromise the patient's ability to adhere to the protocol.
Descrizione

Comorbidity Serious Systemic | Bacterial Infection | Mycoses | Virus Disease | Comorbidity compromises Protocol Compliance

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C0205373
UMLS CUI [2]
C0004623
UMLS CUI [3]
C0026946
UMLS CUI [4]
C0042769
UMLS CUI [5,1]
C0009488
UMLS CUI [5,2]
C2945640
UMLS CUI [5,3]
C0525058
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Similar models

Eligibility Leukemia, Lymphocytic NCT00452257

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Criteria Fulfill
Item
patients are eligible to be included in the study only if they meet all of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Chronic Lymphocytic Leukemia | CD19 Expressing Cell Count Flow Cytometry | CD5 Expressing Cell Measurement Flow Cytometry | CD23 Antigen Flow Cytometry
Item
1. patients with b-cell cll as diagnosed by expression of cd19, cd5, and cd23 by flow cytometry.
boolean
C0023434 (UMLS CUI [1])
C3540683 (UMLS CUI [2,1])
C0016263 (UMLS CUI [2,2])
C3538992 (UMLS CUI [3,1])
C0016263 (UMLS CUI [3,2])
C0123242 (UMLS CUI [4,1])
C0016263 (UMLS CUI [4,2])
Disease Rai Staging System | Indication Therapeutic procedure
Item
2. rai stage iii or iv disease or earlier stage disease with indications for therapy per nci working group criteria (cheson et al. 1996)
boolean
C0012634 (UMLS CUI [1,1])
C1514715 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C0087111 (UMLS CUI [2,2])
Absolute lymphocyte count | Determination of percentage differential white blood cells
Item
3. absolute lymphocyte count > or = to 5,000/microliter, with a lymphocyte wbc differential of > or = to 70%.
boolean
C3544087 (UMLS CUI [1])
C0579194 (UMLS CUI [2])
Platelet Count measurement
Item
4. platelet count >20,000/microliter.
boolean
C0032181 (UMLS CUI [1])
Organ function
Item
5. adequate organ function, including the following:
boolean
C0678852 (UMLS CUI [1])
Liver function | Serum total bilirubin measurement | Alkaline phosphatase measurement | Aspartate aminotransferase measurement | Alanine aminotransferase measurement
Item
hepatic: bilirubin < or = to 1.5 times the upper limit of normal (x uln); alkaline phosphatase (alp), aspartate transaminase (ast), and alanine transaminase (alt) < or = to 2.5 x uln
boolean
C0232741 (UMLS CUI [1])
C1278039 (UMLS CUI [2])
C0201850 (UMLS CUI [3])
C0201899 (UMLS CUI [4])
C0201836 (UMLS CUI [5])
Renal function | Creatinine measurement, serum
Item
renal: serum creatinine < or = to 1.5 x uln.
boolean
C0232804 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Criteria Fulfill
Item
patients will be excluded from the study if they meet any of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Lacking Able to swallow Tablets
Item
1. are unable to swallow tablets.
boolean
C0332268 (UMLS CUI [1,1])
C2712086 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,3])
Carbamazepine Discontinue Unable | Phenobarbital Discontinue Unable | Phenytoin Discontinue Unable
Item
2. are unable to discontinue use of carbamazepine, phenobarbital, and phenytoin.
boolean
C0006949 (UMLS CUI [1,1])
C1444662 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0031412 (UMLS CUI [2,1])
C1444662 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
C0031507 (UMLS CUI [3,1])
C1444662 (UMLS CUI [3,2])
C1299582 (UMLS CUI [3,3])
Pregnancy | Breast Feeding
Item
3. are pregnant or breastfeeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
CNS metastases | Exception Local Therapy Completed | Exception Adrenal Cortex Hormones Discontinued
Item
4. have central nervous system (cns) metastases (unless the patient has completed successful local therapy for cns metastases and has been off of corticosteroids for at least 4 weeks before starting study therapy).
boolean
C0686377 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C1517925 (UMLS CUI [2,2])
C0205197 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C0001617 (UMLS CUI [3,2])
C1444662 (UMLS CUI [3,3])
Comorbidity Serious Systemic | Bacterial Infection | Mycoses | Virus Disease | Comorbidity compromises Protocol Compliance
Item
5. have a serious concomitant systemic disorder (including active bacterial, fungal, or viral infection) that, in the opinion of the investigator, would compromise the patient's ability to adhere to the protocol.
boolean
C0009488 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0205373 (UMLS CUI [1,3])
C0004623 (UMLS CUI [2])
C0026946 (UMLS CUI [3])
C0042769 (UMLS CUI [4])
C0009488 (UMLS CUI [5,1])
C2945640 (UMLS CUI [5,2])
C0525058 (UMLS CUI [5,3])
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