ID

13239

Beschrijving

Prospective, Open-label Tolerability and Safety Monitoring Study of Novantrone in a Selected Cohort of Multiple Sclerosis Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00262314

Link

https://clinicaltrials.gov/show/NCT00262314

Trefwoorden

  1. 25-01-16 25-01-16 -
Geüploaded op

25 januari 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Multiple Sclerosis NCT00262314

Eligibility Multiple Sclerosis NCT00262314

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
platelet count >100,000 cells/µl
Beschrijving

platelet count

Datatype

boolean

Alias
UMLS CUI [1]
C0032181
granulocyte count > 2000 cells/µl
Beschrijving

granulocyte count

Datatype

boolean

Alias
UMLS CUI [1]
C0857490
age 18-65 years
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
negative pregnancy test for female patients who are biologically capable of becoming pregnant, even if they are taking birth control
Beschrijving

pregnancy test

Datatype

boolean

Alias
UMLS CUI [1]
C0032976
for patients of reproductive age, agreement to practice effective contraception throughout the study and for 6 months following the last administration of novantrone®
Beschrijving

contraception

Datatype

boolean

Alias
UMLS CUI [1]
C0700589
signed inform consent.
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
presence of cardiac risk factors:
Beschrijving

cardiac risk factors

Datatype

boolean

Alias
UMLS CUI [1]
C2024776
history of congestive heart failure
Beschrijving

congestive heart failure

Datatype

boolean

Alias
UMLS CUI [1]
C0018802
lvef < 50% determined by echocardiography or muga
Beschrijving

lvef

Datatype

boolean

Alias
UMLS CUI [1]
C0428772
previous treatment with novantrone®, other anthracenediones, or anthracyclines
Beschrijving

anthracenediones, anthracyclines

Datatype

boolean

Alias
UMLS CUI [1]
C0003174
UMLS CUI [2]
C0282564
prior mediastinal radiotherapy or total lymphoidal irradiation
Beschrijving

radiotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C1522449
ast, alt, bilirubin > 2x upper limits of normal
Beschrijving

bilirubin, ast, alt

Datatype

boolean

Alias
UMLS CUI [1]
C1278039
UMLS CUI [2]
C0201899
UMLS CUI [3]
C0201836
severe untreated infection (including current urinary tract infection)
Beschrijving

infection

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0205082
nursing or pregnant women)
Beschrijving

pregnant or nursing

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147

Similar models

Eligibility Multiple Sclerosis NCT00262314

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
platelet count
Item
platelet count >100,000 cells/µl
boolean
C0032181 (UMLS CUI [1])
granulocyte count
Item
granulocyte count > 2000 cells/µl
boolean
C0857490 (UMLS CUI [1])
age
Item
age 18-65 years
boolean
C0001779 (UMLS CUI [1])
pregnancy test
Item
negative pregnancy test for female patients who are biologically capable of becoming pregnant, even if they are taking birth control
boolean
C0032976 (UMLS CUI [1])
contraception
Item
for patients of reproductive age, agreement to practice effective contraception throughout the study and for 6 months following the last administration of novantrone®
boolean
C0700589 (UMLS CUI [1])
informed consent
Item
signed inform consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
cardiac risk factors
Item
presence of cardiac risk factors:
boolean
C2024776 (UMLS CUI [1])
congestive heart failure
Item
history of congestive heart failure
boolean
C0018802 (UMLS CUI [1])
lvef
Item
lvef < 50% determined by echocardiography or muga
boolean
C0428772 (UMLS CUI [1])
anthracenediones, anthracyclines
Item
previous treatment with novantrone®, other anthracenediones, or anthracyclines
boolean
C0003174 (UMLS CUI [1])
C0282564 (UMLS CUI [2])
radiotherapy
Item
prior mediastinal radiotherapy or total lymphoidal irradiation
boolean
C1522449 (UMLS CUI [1])
bilirubin, ast, alt
Item
ast, alt, bilirubin > 2x upper limits of normal
boolean
C1278039 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
C0201836 (UMLS CUI [3])
infection
Item
severe untreated infection (including current urinary tract infection)
boolean
C0009450 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
pregnant or nursing
Item
nursing or pregnant women)
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])

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