ID
4567
Description
ODM derived from http://clinicaltrials.gov/show/NCT00331890
Link
http://clinicaltrials.gov/show/NCT00331890
Keywords
Versions (2)
- 12/11/13 12/11/13 - Martin Dugas
- 4/14/14 4/14/14 - Julian Varghese
Uploaded on
December 11, 2013
DOI
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License
Creative Commons BY-NC 3.0 Legacy
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Eligibility NCT00331890 Acute Stroke. Cerebral Infarction.
Eligibility
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI 2011AA
- CL425201
Description
Patients in coma: patients having a score of >=2 in the items regarding the level of consciousness in the NIHSS (1a)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0009421
- SNOMED CT 2011_0131
- 371632003
- MedDRA 14.1
- 10010071
- LOINC Version 232
- MTHU020645
- ICD-10-CM Version 2010
- R40.20
- ICD-9-CM Version 2011
- 780.01
- UMLS CUI 2011AA
- C1697239
- MedDRA 14.1
- 10065528
- UMLS CUI 2011AA
- CL414978
- UMLS CUI 2011AA
- C0234425
- SNOMED CT 2011_0131
- 6942003
Description
CT or conventional MRI evidence of brain tumor, cerebral edema with a clinically significant mass midline shift with compression of the ventricles, brainstem or cerebellar infarction, subarachnoid and/or intracerebral and/or intraventricular hemorrhage
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0040405
- MedDRA 14.1
- 10011603
- UMLS CUI 2011AA
- C0439858
- SNOMED CT 2011_0131
- 255333006
- UMLS CUI 2011AA
- C0024485
- SNOMED CT 2011_0131
- 113091000
- MedDRA 14.1
- 10028049
- UMLS CUI 2011AA
- C0332120
- SNOMED CT 2011_0131
- 18669006
- UMLS CUI 2011AA
- C0006118
- SNOMED CT 2011_0131
- 126952004
- MedDRA 14.1
- 10061019
- ICD-9-CM Version 2011
- 239.6
- UMLS CUI 2011AA
- C0006114
- SNOMED CT 2011_0131
- 2032001
- MedDRA 14.1
- 10008107
- ICD-10-CM Version 2010
- G93.6
- ICD-9-CM Version 2011
- 348.5
- CTCAE 1105E
- E12650
- UMLS CUI 2011AA
- C0576481
- SNOMED CT 2011_0131
- 299728009
- MedDRA 14.1
- 10069551
- UMLS CUI 2011AA
- C0577559
- SNOMED CT 2011_0131
- 4147007
- MedDRA 14.1
- 10026865
- UMLS CUI 2011AA
- C0205210
- SNOMED CT 2011_0131
- 58147004
- UMLS CUI 2011AA
- C0750502
- SNOMED CT 2011_0131
- 386134007
- UMLS CUI 2011AA
- C0332459
- SNOMED CT 2011_0131
- 71173004
- UMLS CUI 2011AA
- C0007799
- SNOMED CT 2011_0131
- 35764002
- LOINC Version 232
- MTHU024384
- UMLS CUI 2011AA
- C0521542
- SNOMED CT 2011_0131
- 95457000
- MedDRA 14.1
- 10006147
- UMLS CUI 2011AA
- C0236073
- SNOMED CT 2011_0131
- 95460007
- MedDRA 14.1
- 10008034
- UMLS CUI 2011AA
- C0038525
- SNOMED CT 2011_0131
- 21454007
- MedDRA 14.1
- 10042316
- ICD-9-CM Version 2011
- 430
- UMLS CUI 2011AA
- C2937358
- SNOMED CT 2011_0131
- 274100004
- MedDRA 14.1
- 10008111
- ICD-9-CM Version 2011
- 431
- UMLS CUI 2011AA
- C0240059
- SNOMED CT 2011_0131
- 23276006
- MedDRA 14.1
- 10022840
Description
History of ventricular dysrhythmias, acute myocardial infarction within 72 hours prior to enrolment, unstable angina, decompensated congestive heart failure or any other acute, severe, uncontrollable or sustained cardiovascular condition that, in the Investigator's opinion, may interfere with effective participation in the study
Data type
boolean
Alias
- UMLS CUI 2011AA
- CL421546
- SNOMED CT 2011_0131
- 392521001
- UMLS CUI 2011AA
- C0085612
- SNOMED CT 2011_0131
- 44103008
- MedDRA 14.1
- 10047281
- ICD-10-CM Version 2010
- I49.01
- CTCAE 1105E
- E10230
- UMLS CUI 2011AA
- C0155626
- SNOMED CT 2011_0131
- 57054005
- MedDRA 14.1
- 10000891
- ICD-10-CM Version 2010
- I21
- ICD-9-CM Version 2011
- 410
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C1516879
- UMLS CUI 2011AA
- C0002965
- SNOMED CT 2011_0131
- 4557003
- MedDRA 14.1
- 10002388
- ICD-10-CM Version 2010
- I20.0
- ICD-9-CM Version 2011
- 411.1
- UMLS CUI 2011AA
- C0205434
- SNOMED CT 2011_0131
- 5650002
- UMLS CUI 2011AA
- C0018802
- SNOMED CT 2011_0131
- 42343007
- MedDRA 14.1
- 10007559
- LOINC Version 232
- MTHU020787
- ICD-10-CM Version 2010
- I50.9
- ICD-9-CM Version 2011
- 428.0
- UMLS CUI 2011AA
- C0007222
- SNOMED CT 2011_0131
- 105980002
- MedDRA 14.1
- 10007649
- ICD-9-CM Version 2011
- 429.2
- UMLS CUI 2011AA
- C0205178
- SNOMED CT 2011_0131
- 272118002
- UMLS CUI 2011AA
- C0205082
- SNOMED CT 2011_0131
- 24484000
- UMLS CUI 2011AA
- C0205318
- SNOMED CT 2011_0131
- 19032002
- UMLS CUI 2011AA
- C0443318
- SNOMED CT 2011_0131
- 263892007
- UMLS CUI 2011AA
- C0521102
- SNOMED CT 2011_0131
- 78235001
- UMLS CUI 2011AA
- C1704419
- SNOMED CT 2011_0131
- 254648000
- UMLS CUI 2011AA
- C0679823
- HL7 V3 2006_05
- PART
- UMLS CUI 2011AA
- C0008976
- SNOMED CT 2011_0131
- 110465008
Description
Previous disorders that may confound the interpretation of the neurological scales
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205156
- SNOMED CT 2011_0131
- 9130008
- UMLS CUI 2011AA
- C0012634
- SNOMED CT 2011_0131
- 64572001
- UMLS CUI 2011AA
- C0459471
- SNOMED CT 2011_0131
- 280452008
- LOINC Version 232
- MTHU003869
- UMLS CUI 2011AA
- C0205494
- SNOMED CT 2011_0131
- 1199008
- LOINC Version 232
- MTHU031871
- UMLS CUI 2011AA
- C0349674
- SNOMED CT 2011_0131
- 278111002
Description
Drug addiction-related disorders
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1510472
- SNOMED CT 2011_0131
- 191816009
- MedDRA 14.1
- 10013663
- ICD-9-CM Version 2011
- 304
- UMLS CUI 2011AA
- C0012634
- SNOMED CT 2011_0131
- 64572001
Description
Pre existing dementia, when dementia implies a disability, measured as an score of >=2 in the previous MRS
Data type
boolean
Alias
- UMLS CUI 2011AA
- C2347662
- UMLS CUI 2011AA
- C0497327
- SNOMED CT 2011_0131
- 52448006
- MedDRA 14.1
- 10012267
- ICD-10-CM Version 2010
- F03
- ICD-9-CM Version 2011
- 290
- UMLS CUI 2011AA
- C0231170
- SNOMED CT 2011_0131
- 21134002
- MedDRA 14.1
- 10013050
- HL7 V3 2006_05
- DIS
- UMLS CUI 2011AA
- C0449820
- SNOMED CT 2011_0131
- 246262008
- LOINC Version 232
- MTHU024701
- UMLS CUI 2011AA
- C0205156
- SNOMED CT 2011_0131
- 9130008
- UMLS CUI 2011AA
- CL423500
Description
Pre existing medical condition that, in the Investigator's opinion, may interfere with the patient's suitability and participation in the study
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0262926
- SNOMED CT 2011_0131
- 417662000
- LOINC Version 232
- MTHU027722
- UMLS CUI 2011AA
- C0521102
- SNOMED CT 2011_0131
- 78235001
- UMLS CUI 2011AA
- C0679823
- UMLS CUI 2011AA
- C0008976
- SNOMED CT 2011_0131
- 110465008
Description
Patients participating in another clinical trial or receiving a non-approved drug (clinical investigational drug) <30 days prior to screening
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0679823
- UMLS CUI 2011AA
- C0008976
- SNOMED CT 2011_0131
- 110465008
- UMLS CUI 2011AA
- C1514756
- UMLS CUI 2011AA
- C0205210
- SNOMED CT 2011_0131
- 58147004
- UMLS CUI 2011AA
- C0013230
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C1409616
Description
Patients under current treatment with citicoline
Data type
boolean
Alias
- UMLS CUI 2011AA
- C2827774
- UMLS CUI 2011AA
- C0010725
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Eligibility
- StudyEvent: Eligibility
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288556008 (SNOMED CT 2011_0131)
C1516879 (UMLS CUI 2011AA)
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110465008 (SNOMED CT 2011_0131)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
C1514756 (UMLS CUI 2011AA)
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58147004 (SNOMED CT 2011_0131)
C0013230 (UMLS CUI 2011AA)
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