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Informações:
Falhas:
ID
6457
Descrição
ODM derived from http://clinicaltrials.gov/show/NCT00190047
Link
http://clinicaltrials.gov/show/NCT00190047
Palavras-chave
Versões (2)
- 22/12/2014 22/12/2014 - Sarah Schulze Sünninghausen
- 11/01/2015 11/01/2015 - Sarah Schulze Sünninghausen
Transferido a
22 de dezembro de 2014
DOI
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Licença
Creative Commons BY-NC 3.0 Legacy
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Eligibility NCT00190047 Stroke
Similar models
Eligibility
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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)
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)
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)
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
Patients with a brain (intracerebral or subarachnoid) hemorrhage per screening computed tomography scan
integer
C2238497 (UMLS CUI-1)
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)
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)
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)
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)
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)
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)
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)
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)
C0020649 (UMLS CUI-2)
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)
C0023895 (UMLS CUI-2)
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)
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
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)
C0085762 (UMLS CUI-2)
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)
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)
Age
Item
Age
string
C0001779 (UMLS CUI)
102518004 (SNOMED CT 2010_0731)
102518004 (SNOMED CT 2010_0731)
Diagnosis
Item
Diagnosis
string
Ischemic stroke
Item
Ischemic stroke
string
C0948008 (UMLS CUI)
422504002 (SNOMED CT 2010_0731)
10055221 (MedDRA 13.1)
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)
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)
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)
246564008 (SNOMED CT 2010_0731)
R41.4 (ICD-10-CM Version 2010)
Onset
Item
Onset
string
C0332162 (UMLS CUI)
77374008 (SNOMED CT 2010_0731)
77374008 (SNOMED CT 2010_0731)
NIH stroke scale
Item
NIH-SS
string
C1697238 (UMLS CUI)
10065527 (MedDRA 13.1)
10065527 (MedDRA 13.1)
Deficits, Neurologic
Item
Neurologic deficit
string
C0521654 (UMLS CUI)
264552009 (SNOMED CT 2010_0731)
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)
405078008 (SNOMED CT 2010_0731)
Haemorrhagic stroke
Item
Brain hemorrhage
string
C0553692 (UMLS CUI)
230706003 (SNOMED CT 2010_0731)
10019016 (MedDRA 13.1)
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)
10057167 (MedDRA 13.1)
Cardiopulmonary Bypass
Item
Cardiopulmonary bypass operation
string
C0007202 (UMLS CUI)
63697000 (SNOMED CT 2010_0731)
10066123 (MedDRA 13.1)
63697000 (SNOMED CT 2010_0731)
10066123 (MedDRA 13.1)
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)
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)
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)
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)
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)
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)
69480007 (SNOMED CT 2010_0731)
10017687 (MedDRA 13.1)
2324-2 (LOINC Version 232)
Platelet count
Item
Platelet count - finding
string
pregnant
Item
pregnant
string
C0549206 (UMLS CUI)
10036586 (MedDRA 13.1)
10036586 (MedDRA 13.1)
Lactation
Item
Breast feeding, Nursing
string
C0006147 (UMLS CUI)
10006247 (MedDRA 13.1)
10006247 (MedDRA 13.1)
Contraception
Item
Contraception
string
C0700589 (UMLS CUI)
146680009 (SNOMED CT 2010_0731)
10010808 (MedDRA 13.1)
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)
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)
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)