ID

6457

Beschrijving

ODM derived from http://clinicaltrials.gov/show/NCT00190047

Link

http://clinicaltrials.gov/show/NCT00190047

Trefwoorden

Versies (2)
  1. 22-12-14 22-12-14 - Sarah Schulze Sünninghausen
  2. 11-01-15 11-01-15 - Sarah Schulze Sünninghausen
Geüploaded op

22 december 2014

DOI

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Licentie

Creative Commons BY-NC 3.0 Legacy
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Eligibility NCT00190047 Stroke

Engels

Eligibility

1 Formulieren  
  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion Criteria
Beschrijving

Inclusion Criteria

18 Years to 85 Years
Beschrijving

Age

Datatype

integer

Alias
UMLS CUI-1
C0001779
Patients with ischemic stroke, (that is, stroke that results from a blockage of blood flow to part of the brain), which is accompanied by language dysfunction (e.g. inability to understand speech), visual field defect or inattention to one side of the body or the space around the patient
Beschrijving

ischemic stroke with language dysfunction, visual field defect or inattention to one side of the body

Datatype

integer

Alias
UMLS CUI-1
C0948008
Patients in whom the study treatment can start no less than 1 and not more than 9 hours after the stroke's onset
Beschrijving

start of study treatment between 1 and 9 hours after stroke onset

Datatype

boolean

Patients with moderate-severe degree of neurological deficit in the 9 hours after stroke onset (defined as NIHSS score of 7 to 20)
Beschrijving

moderate-severe neurological deficit

Datatype

integer

Alias
UMLS CUI-1
C0521654
Patients that can understand the requirements of the study and are willing to provide written informed consent (If the subject is incapacitated, informed consent will be sought from a legally acceptable representative.)
Beschrijving

informed consent

Datatype

integer

Alias
UMLS CUI-1
C2348568
Exclusion Criteria
Beschrijving

Exclusion Criteria

Patients with a brain (intracerebral or subarachnoid) hemorrhage per screening computed tomography scan
Beschrijving

brain hemorrhage

Datatype

integer

Alias
UMLS CUI-1
C2238497
candidates for thrombolytic therapy for the current stroke
Beschrijving

candidates for thrombolytic therapy

Datatype

integer

Alias
UMLS CUI-1
C0040044
patients having a mental impairment that renders them incapable to understand the study's requirements
Beschrijving

patients with mental impairment

Datatype

integer

Alias
UMLS CUI-1
C1306341
patients with other diseases that in the investigator's opinion may lead, independently of the current stroke, to further deterioration in the subject's neurological status during the trial period, or may confuse the evaluation of the present stroke
Beschrijving

other diseases

Datatype

integer

Alias
UMLS CUI-1
C0009488
Patients likely to undergo a procedure involving cardiopulmonary bypass during the study period
Beschrijving

cardiopulmonary bypass

Datatype

integer

Alias
UMLS CUI-1
C0007202
Patients with medical conditions that may not enable them to complete the study (e.g life-threatening diseases,)
Beschrijving

other medical conditions

Datatype

integer

Alias
UMLS CUI-1
C0001314
Patients whose condition improves already during the screening period
Beschrijving

Patients whose condition improves already during the screening period

Datatype

integer

Alias
UMLS CUI-1
C0184511
Patients who already have functional limitations before the present study (retrospective Modified Rankin Scale score of >3)
Beschrijving

Rankin Scale Score >3

Datatype

integer

Alias
UMLS CUI-1
C0521987
Patients who suffered a stroke within the past 90 days that seems to have been in the same brain region as the current acute stroke
Beschrijving

stroke within the past 90 days in the same brain region

Datatype

boolean

Patients with severe hypertension (systolic BP >210 mm Hg or diastolic BP >120 mm Hg) or hypotension (systolic BP <90 mm Hg),
Beschrijving

severe hypertension or hypotension

Datatype

integer

Alias
UMLS CUI-1
C0020538
UMLS CUI-2
C0020649
Patients with significant history of renal or liver disease(s) (serum creatinine of > 2.0 mg/dL, alanine aminotransferase, aspartate aminotransferase, or gamma-glutamyl transferase values of > threefold the upper normal limit)
Beschrijving

renal or liver disease

Datatype

integer

Alias
UMLS CUI-1
C0022658
UMLS CUI-2
C0023895
Patients with a platelet count of <100,000/mm3
Beschrijving

platelet count of <100,000/mm3

Datatype

integer

Alias
UMLS CUI-1
C0040034
Female patients of childbearing potential who are not using adequate and effective birth control measures or who are pregnant or lactating (the screening evaluation of female subjects of childbearing potential will include a serum pregnancy test.)
Beschrijving

pregnancy, lactation, no contraception

Datatype

integer

Patients who are users of addictive agents, or alcoholics
Beschrijving

Patients who are users of addictive agents, or alcoholics

Datatype

integer

Alias
UMLS CUI-1
C0813966
UMLS CUI-2
C0085762
Patients who have received an investigational drug within the 90 days before the present stroke or such that are past recipients of DP-b99
Beschrijving

Other trials

Datatype

integer

Alias
UMLS CUI-1
C1548937
Medical concepts
Beschrijving

Medical concepts

Age
Beschrijving

Age

Datatype

string

Alias
UMLS CUI
C0001779
SNOMED CT 2010_0731
102518004
Diagnosis
Beschrijving

Diagnosis

Datatype

string

Alias
UMLS CUI
C0011900
SNOMED CT 2010_0731
439401001
LOINC Version 232
MTHU008876
Ischemic stroke
Beschrijving

Ischemic stroke

Datatype

string

Alias
UMLS CUI
C0948008
SNOMED CT 2010_0731
422504002
MedDRA 13.1
10055221
Disorder of language
Beschrijving

Language Disorders

Datatype

string

Alias
UMLS CUI
C0023015
SNOMED CT 2010_0731
62305002
ICD-10-CM Version 2010
F80.9
Visual field defect
Beschrijving

Scotoma

Datatype

string

Alias
UMLS CUI
C0036454
SNOMED CT 2010_0731
12184005, 23388006
MedDRA 13.1
10047555, 10039729
ICD-10-CM Version 2010
H53.4
ICD-9-CM Version 2011
368.4
Hemi-inattention
Beschrijving

Neglect of one side of body

Datatype

string

Alias
UMLS CUI
C0422887
SNOMED CT 2010_0731
246564008
ICD-10-CM Version 2010
R41.4
Onset
Beschrijving

Onset

Datatype

string

Alias
UMLS CUI
C0332162
SNOMED CT 2010_0731
77374008
NIH-SS
Beschrijving

NIH stroke scale

Datatype

string

Alias
UMLS CUI
C1697238
MedDRA 13.1
10065527
Neurologic deficit
Beschrijving

Deficits, Neurologic

Datatype

string

Alias
UMLS CUI
C0521654
SNOMED CT 2010_0731
264552009
Informed Consent
Beschrijving

Informed Consent

Datatype

string

Alias
UMLS CUI
C0021430
Compliance
Beschrijving

Compliance

Datatype

string

Alias
UMLS CUI
C1321605
SNOMED CT 2010_0731
405078008
Brain hemorrhage
Beschrijving

Haemorrhagic stroke

Datatype

string

Alias
UMLS CUI
C0553692
SNOMED CT 2010_0731
230706003
MedDRA 13.1
10019016
Therapeutic procedure
Beschrijving

Therapeutic procedure

Datatype

string

Alias
UMLS CUI
C0087111
Medication
Beschrijving

Pharmaceutical Preparations

Datatype

string

Alias
UMLS CUI
C0013227
Mental impairment disorders
Beschrijving

Mental impairment disorders

Datatype

string

Alias
UMLS CUI
C1112722
MedDRA 13.1
10057167
Cardiopulmonary bypass operation
Beschrijving

Cardiopulmonary Bypass

Datatype

string

Alias
UMLS CUI
C0007202
SNOMED CT 2010_0731
63697000
MedDRA 13.1
10066123
Life expectancy
Beschrijving

Life expectancy

Datatype

string

Alias
UMLS CUI
C0023671
LOINC Version 232
LP75025-4
Rankin score
Beschrijving

Rankin score

Datatype

string

Alias
UMLS CUI
CL423500
Hypertensive disease
Beschrijving

Hypertension

Datatype

string

Alias
UMLS CUI
C0020538
SNOMED CT 2010_0731
38341003
MedDRA 13.1
10020772
LOINC Version 232
MTHU020789
ICD-10-CM Version 2010
I10
ICD-9-CM Version 2011
997.91
CTCAE Version 4.03
E13785
Hypotension
Beschrijving

Low blood pressure

Datatype

string

Alias
UMLS CUI
C0020649
SNOMED CT 2010_0731
45007003
MedDRA 13.1
10003146
ICD-10-CM Version 2010
I95
ICD-9-CM Version 2011
458
Creatinine
Beschrijving

Creatinine

Datatype

string

Alias
UMLS CUI
C0010294
SNOMED CT 2010_0731
15373003
MedDRA 13.1
10011358
LOINC Version 232
38483-4
GPT (Serum)
Beschrijving

ALT

Datatype

string

Alias
UMLS CUI
C0001899
SNOMED CT 2010_0731
56935002
MedDRA 13.1
10001844
GOT (Serum)
Beschrijving

AST

Datatype

string

Alias
UMLS CUI
C0004002
SNOMED CT 2010_0731
26091008
MedDRA 13.1
10003543
Gamma Glutamyl Transpeptidase Measurement
Beschrijving

GGT

Datatype

string

Alias
UMLS CUI
C0202035
SNOMED CT 2010_0731
69480007
MedDRA 13.1
10017687
LOINC Version 232
2324-2
Platelet count - finding
Beschrijving

Platelet count

Datatype

string

Alias
UMLS CUI
C1287267
SNOMED CT 2010_0731
365632008
LOINC Version 232
777-3
pregnant
Beschrijving

pregnant

Datatype

string

Alias
UMLS CUI
C0549206
MedDRA 13.1
10036586
Breast feeding, Nursing
Beschrijving

Lactation

Datatype

string

Alias
UMLS CUI
C0006147
MedDRA 13.1
10006247
Contraception
Beschrijving

Contraception

Datatype

string

Alias
UMLS CUI
C0700589
SNOMED CT 2010_0731
146680009
MedDRA 13.1
10010808
Alcohol abuse
Beschrijving

Alcohol abuse

Datatype

string

Alias
UMLS CUI
C0085762
SNOMED CT 2010_0731
15167005
MedDRA 13.1
10001584
LOINC Version 232
LP36309-0
ICD-10-CM Version 2010
F10.1
ICD-9-CM Version 2011
305.0
Drug abuse
Beschrijving

Drug abuse

Datatype

string

Alias
UMLS CUI
C0013146
SNOMED CT 2010_0731
26416006
MedDRA 13.1
10013654
LOINC Version 232
LP36310-8
ICD-9-CM Version 2011
305.90
Enrollment
Beschrijving

Enrollment

Datatype

string

Alias
UMLS CUI
C2348568
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Similar models

Eligibility

1 Formulieren
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Inclusion Criteria
Item
18 Years to 85 Years
integer
C0001779 (UMLS CUI-1)
Age
Code List
18 Years to 85 Years
CL Item
yes (1)
CL Item
no (2)
Item
Patients with ischemic stroke, (that is, stroke that results from a blockage of blood flow to part of the brain), which is accompanied by language dysfunction (e.g. inability to understand speech), visual field defect or inattention to one side of the body or the space around the patient
integer
C0948008 (UMLS CUI-1)
ischemic stroke with language dysfunction, visual field defect or inattention to one side of the body
Code List
Patients with ischemic stroke, (that is, stroke that results from a blockage of blood flow to part of the brain), which is accompanied by language dysfunction (e.g. inability to understand speech), visual field defect or inattention to one side of the body or the space around the patient
CL Item
yes (1)
CL Item
no (2)
start of study treatment between 1 and 9 hours after stroke onset
Item
Patients in whom the study treatment can start no less than 1 and not more than 9 hours after the stroke's onset
boolean
Item
Patients with moderate-severe degree of neurological deficit in the 9 hours after stroke onset (defined as NIHSS score of 7 to 20)
integer
C0521654 (UMLS CUI-1)
moderate-severe neurological deficit
Code List
Patients with moderate-severe degree of neurological deficit in the 9 hours after stroke onset (defined as NIHSS score of 7 to 20)
CL Item
yes (1)
CL Item
no (2)
Item
Patients that can understand the requirements of the study and are willing to provide written informed consent (If the subject is incapacitated, informed consent will be sought from a legally acceptable representative.)
integer
C2348568 (UMLS CUI-1)
informed consent
Code List
Patients that can understand the requirements of the study and are willing to provide written informed consent (If the subject is incapacitated, informed consent will be sought from a legally acceptable representative.)
CL Item
yes (1)
CL Item
no (2)
Item Group
Exclusion Criteria
Item
Patients with a brain (intracerebral or subarachnoid) hemorrhage per screening computed tomography scan
integer
C2238497 (UMLS CUI-1)
brain hemorrhage
Code List
Patients with a brain (intracerebral or subarachnoid) hemorrhage per screening computed tomography scan
CL Item
yes (1)
CL Item
no (2)
Item
candidates for thrombolytic therapy for the current stroke
integer
C0040044 (UMLS CUI-1)
candidates for thrombolytic therapy
Code List
candidates for thrombolytic therapy for the current stroke
CL Item
yes (1)
CL Item
no (2)
Item
patients having a mental impairment that renders them incapable to understand the study's requirements
integer
C1306341 (UMLS CUI-1)
patients with mental impairment
Code List
patients having a mental impairment that renders them incapable to understand the study's requirements
CL Item
yes (1)
CL Item
no (2)
Item
patients with other diseases that in the investigator's opinion may lead, independently of the current stroke, to further deterioration in the subject's neurological status during the trial period, or may confuse the evaluation of the present stroke
integer
C0009488 (UMLS CUI-1)
other diseases
Code List
patients with other diseases that in the investigator's opinion may lead, independently of the current stroke, to further deterioration in the subject's neurological status during the trial period, or may confuse the evaluation of the present stroke
CL Item
yes (1)
CL Item
no (2)
Item
Patients likely to undergo a procedure involving cardiopulmonary bypass during the study period
integer
C0007202 (UMLS CUI-1)
cardiopulmonary bypass
Code List
Patients likely to undergo a procedure involving cardiopulmonary bypass during the study period
CL Item
yes (1)
CL Item
no (2)
Item
Patients with medical conditions that may not enable them to complete the study (e.g life-threatening diseases,)
integer
C0001314 (UMLS CUI-1)
other medical conditions
Code List
Patients with medical conditions that may not enable them to complete the study (e.g life-threatening diseases,)
CL Item
yes (1)
CL Item
no (2)
Item
Patients whose condition improves already during the screening period
integer
C0184511 (UMLS CUI-1)
Patients whose condition improves already during the screening period
Code List
Patients whose condition improves already during the screening period
CL Item
yes (1)
CL Item
no (2)
Item
Patients who already have functional limitations before the present study (retrospective Modified Rankin Scale score of >3)
integer
C0521987 (UMLS CUI-1)
Rankin Scale Score >3
Code List
Patients who already have functional limitations before the present study (retrospective Modified Rankin Scale score of >3)
CL Item
yes (1)
CL Item
no (2)
stroke within the past 90 days in the same brain region
Item
Patients who suffered a stroke within the past 90 days that seems to have been in the same brain region as the current acute stroke
boolean
Item
Patients with severe hypertension (systolic BP >210 mm Hg or diastolic BP >120 mm Hg) or hypotension (systolic BP <90 mm Hg),
integer
C0020538 (UMLS CUI-1)
C0020649 (UMLS CUI-2)
severe hypertension or hypotension
Code List
Patients with severe hypertension (systolic BP >210 mm Hg or diastolic BP >120 mm Hg) or hypotension (systolic BP <90 mm Hg),
CL Item
yes (1)
CL Item
no (2)
Item
Patients with significant history of renal or liver disease(s) (serum creatinine of > 2.0 mg/dL, alanine aminotransferase, aspartate aminotransferase, or gamma-glutamyl transferase values of > threefold the upper normal limit)
integer
C0022658 (UMLS CUI-1)
C0023895 (UMLS CUI-2)
renal or liver disease
Code List
Patients with significant history of renal or liver disease(s) (serum creatinine of > 2.0 mg/dL, alanine aminotransferase, aspartate aminotransferase, or gamma-glutamyl transferase values of > threefold the upper normal limit)
CL Item
yes (1)
CL Item
no (2)
Item
Patients with a platelet count of <100,000/mm3
integer
C0040034 (UMLS CUI-1)
platelet count of <100,000/mm3
Code List
Patients with a platelet count of <100,000/mm3
CL Item
yes (1)
CL Item
no (2)
Item
Female patients of childbearing potential who are not using adequate and effective birth control measures or who are pregnant or lactating (the screening evaluation of female subjects of childbearing potential will include a serum pregnancy test.)
integer
pregnancy, lactation, no contraception
Code List
Female patients of childbearing potential who are not using adequate and effective birth control measures or who are pregnant or lactating (the screening evaluation of female subjects of childbearing potential will include a serum pregnancy test.)
CL Item
yes (1)
CL Item
no (2)
Item
Patients who are users of addictive agents, or alcoholics
integer
C0813966 (UMLS CUI-1)
C0085762 (UMLS CUI-2)
Patients who are users of addictive agents, or alcoholics
Code List
Patients who are users of addictive agents, or alcoholics
CL Item
yes (1)
CL Item
no (2)
Item
Patients who have received an investigational drug within the 90 days before the present stroke or such that are past recipients of DP-b99
integer
C1548937 (UMLS CUI-1)
Other trials
Code List
Patients who have received an investigational drug within the 90 days before the present stroke or such that are past recipients of DP-b99
CL Item
yes (1)
CL Item
no (2)
Item Group
Medical concepts
Age
Item
Age
string
C0001779 (UMLS CUI)
102518004 (SNOMED CT 2010_0731)
Diagnosis
Item
Diagnosis
string
C0011900 (UMLS CUI)
439401001 (SNOMED CT 2010_0731)
MTHU008876 (LOINC Version 232)
Ischemic stroke
Item
Ischemic stroke
string
C0948008 (UMLS CUI)
422504002 (SNOMED CT 2010_0731)
10055221 (MedDRA 13.1)
Language Disorders
Item
Disorder of language
string
C0023015 (UMLS CUI)
62305002 (SNOMED CT 2010_0731)
F80.9 (ICD-10-CM Version 2010)
Scotoma
Item
Visual field defect
string
C0036454 (UMLS CUI)
12184005, 23388006 (SNOMED CT 2010_0731)
10047555, 10039729 (MedDRA 13.1)
H53.4 (ICD-10-CM Version 2010)
368.4 (ICD-9-CM Version 2011)
Neglect of one side of body
Item
Hemi-inattention
string
C0422887 (UMLS CUI)
246564008 (SNOMED CT 2010_0731)
R41.4 (ICD-10-CM Version 2010)
Onset
Item
Onset
string
C0332162 (UMLS CUI)
77374008 (SNOMED CT 2010_0731)
NIH stroke scale
Item
NIH-SS
string
C1697238 (UMLS CUI)
10065527 (MedDRA 13.1)
Deficits, Neurologic
Item
Neurologic deficit
string
C0521654 (UMLS CUI)
264552009 (SNOMED CT 2010_0731)
Informed Consent
Item
Informed Consent
string
C0021430 (UMLS CUI)
Compliance
Item
Compliance
string
C1321605 (UMLS CUI)
405078008 (SNOMED CT 2010_0731)
Haemorrhagic stroke
Item
Brain hemorrhage
string
C0553692 (UMLS CUI)
230706003 (SNOMED CT 2010_0731)
10019016 (MedDRA 13.1)
Therapeutic procedure
Item
Therapeutic procedure
string
C0087111 (UMLS CUI)
Pharmaceutical Preparations
Item
Medication
string
C0013227 (UMLS CUI)
Mental impairment disorders
Item
Mental impairment disorders
string
C1112722 (UMLS CUI)
10057167 (MedDRA 13.1)
Cardiopulmonary Bypass
Item
Cardiopulmonary bypass operation
string
C0007202 (UMLS CUI)
63697000 (SNOMED CT 2010_0731)
10066123 (MedDRA 13.1)
Life expectancy
Item
Life expectancy
string
C0023671 (UMLS CUI)
LP75025-4 (LOINC Version 232)
Rankin score
Item
Rankin score
string
CL423500 (UMLS CUI)
Hypertension
Item
Hypertensive disease
string
C0020538 (UMLS CUI)
38341003 (SNOMED CT 2010_0731)
10020772 (MedDRA 13.1)
MTHU020789 (LOINC Version 232)
I10 (ICD-10-CM Version 2010)
997.91 (ICD-9-CM Version 2011)
E13785 (CTCAE Version 4.03)
Low blood pressure
Item
Hypotension
string
C0020649 (UMLS CUI)
45007003 (SNOMED CT 2010_0731)
10003146 (MedDRA 13.1)
I95 (ICD-10-CM Version 2010)
458 (ICD-9-CM Version 2011)
Creatinine
Item
Creatinine
string
C0010294 (UMLS CUI)
15373003 (SNOMED CT 2010_0731)
10011358 (MedDRA 13.1)
38483-4 (LOINC Version 232)
ALT
Item
GPT (Serum)
string
C0001899 (UMLS CUI)
56935002 (SNOMED CT 2010_0731)
10001844 (MedDRA 13.1)
AST
Item
GOT (Serum)
string
C0004002 (UMLS CUI)
26091008 (SNOMED CT 2010_0731)
10003543 (MedDRA 13.1)
GGT
Item
Gamma Glutamyl Transpeptidase Measurement
string
C0202035 (UMLS CUI)
69480007 (SNOMED CT 2010_0731)
10017687 (MedDRA 13.1)
2324-2 (LOINC Version 232)
Platelet count
Item
Platelet count - finding
string
C1287267 (UMLS CUI)
365632008 (SNOMED CT 2010_0731)
777-3 (LOINC Version 232)
pregnant
Item
pregnant
string
C0549206 (UMLS CUI)
10036586 (MedDRA 13.1)
Lactation
Item
Breast feeding, Nursing
string
C0006147 (UMLS CUI)
10006247 (MedDRA 13.1)
Contraception
Item
Contraception
string
C0700589 (UMLS CUI)
146680009 (SNOMED CT 2010_0731)
10010808 (MedDRA 13.1)
Alcohol abuse
Item
Alcohol abuse
string
C0085762 (UMLS CUI)
15167005 (SNOMED CT 2010_0731)
10001584 (MedDRA 13.1)
LP36309-0 (LOINC Version 232)
F10.1 (ICD-10-CM Version 2010)
305.0 (ICD-9-CM Version 2011)
Drug abuse
Item
Drug abuse
string
C0013146 (UMLS CUI)
26416006 (SNOMED CT 2010_0731)
10013654 (MedDRA 13.1)
LP36310-8 (LOINC Version 232)
305.90 (ICD-9-CM Version 2011)
Enrollment
Item
Enrollment
string
C2348568 (UMLS CUI)
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