ID

4435

Descripción

ODM derived from http://clinicaltrials.gov/show/NCT00771927

Link

http://clinicaltrials.gov/show/NCT00771927

Palabras clave

Versiones (1)
  1. 9/12/13 9/12/13 - Martin Dugas
Subido en

9 de diciembre de 2013

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility NCT00771927 Epilepsies, Partial

Alemán Inglés

Eligibility

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility
Einschlusskriterien
Descripción

Einschlusskriterien

Alias
UMLS CUI 2011AA
CL425202
Alter mindestens 16 Jahre
Descripción

age at least 16 Years

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0001779
SNOMED CT 2011_0131
397669002
This study includes any subject 16 years or older who has an epilepsy diagnosis with partial on-set seizures, and whose seizure activity is uncontrolled on current therapy
Descripción

This study includes any subject 16 years or older who has an epilepsy diagnosis with partial on-set seizures, and whose seizure activity is uncontrolled on current therapy

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0014544
SNOMED CT 2011_0131
84757009
MedDRA 14.1
10015037
LOINC Version 232
MTHU020586
ICD-10-CM Version 2010
G40.9
ICD-9-CM Version 2011
345.9
UMLS CUI 2011AA
C0011900
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
UMLS CUI 2011AA
C0014547
SNOMED CT 2011_0131
29753000
MedDRA 14.1
10065336
UMLS CUI 2011AA
C1148454
LOINC Version 232
MTHU015069
UMLS CUI 2011AA
C0205318
SNOMED CT 2011_0131
19032002
UMLS CUI 2011AA
C2827774
Patients who are prescribed Vimpat or any other add-on AED may be included in the study.
Descripción

Patients who are prescribed Vimpat or any other add-on AED may be included in the study.

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0033080
SNOMED CT 2011_0131
16076005
UMLS CUI 2011AA
C1311230
SNOMED CT 2011_0131
441532003
LOINC Version 232
MTHU035825
UMLS CUI 2011AA
C0205394
SNOMED CT 2011_0131
74964007
UMLS CUI 2011AA
C0003299
SNOMED CT 2011_0131
255632006
LOINC Version 232
MTHU006781
The initiation of an add-on AED therapy can not be more than 2 days before the patient's start of the study.
Descripción

The initiation of an add-on AED therapy can not be more than 2 days before the patient's start of the study.

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C1704686
UMLS CUI 2011AA
C0003299
SNOMED CT 2011_0131
255632006
LOINC Version 232
MTHU006781
UMLS CUI 2011AA
C0039798
UMLS CUI 2011AA
C0439090
SNOMED CT 2011_0131
276137008
HL7 V3 2006_05
LE
UMLS CUI 2011AA
C0205448
SNOMED CT 2011_0131
19338005
UMLS CUI 2011AA
C0439228
SNOMED CT 2011_0131
258703001
HL7 V3 2006_05
D
UMLS CUI 2011AA
C0332152
SNOMED CT 2011_0131
288556008
UMLS CUI 2011AA
C0030705
SNOMED CT 2011_0131
116154003
UMLS CUI 2011AA
C2348558
Ausschlusskriterien
Descripción

Ausschlusskriterien

Alias
UMLS CUI 2011AA
CL425201
No Information Available
Descripción

N/A

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C1546437
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Similar models

Eligibility

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Einschlusskriterien
CL425202 (UMLS CUI 2011AA)
age at least 16 Years
Item
Alter mindestens 16 Jahre
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
This study includes any subject 16 years or older who has an epilepsy diagnosis with partial on-set seizures, and whose seizure activity is uncontrolled on current therapy
Item
This study includes any subject 16 years or older who has an epilepsy diagnosis with partial on-set seizures, and whose seizure activity is uncontrolled on current therapy
boolean
C0014544 (UMLS CUI 2011AA)
84757009 (SNOMED CT 2011_0131)
10015037 (MedDRA 14.1)
MTHU020586 (LOINC Version 232)
G40.9 (ICD-10-CM Version 2010)
345.9 (ICD-9-CM Version 2011)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0014547 (UMLS CUI 2011AA)
29753000 (SNOMED CT 2011_0131)
10065336 (MedDRA 14.1)
C1148454 (UMLS CUI 2011AA)
MTHU015069 (LOINC Version 232)
C0205318 (UMLS CUI 2011AA)
19032002 (SNOMED CT 2011_0131)
C2827774 (UMLS CUI 2011AA)
Patients who are prescribed Vimpat or any other add-on AED may be included in the study.
Item
Patients who are prescribed Vimpat or any other add-on AED may be included in the study.
boolean
C0033080 (UMLS CUI 2011AA)
16076005 (SNOMED CT 2011_0131)
C1311230 (UMLS CUI 2011AA)
441532003 (SNOMED CT 2011_0131)
MTHU035825 (LOINC Version 232)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C0003299 (UMLS CUI 2011AA)
255632006 (SNOMED CT 2011_0131)
MTHU006781 (LOINC Version 232)
The initiation of an add-on AED therapy can not be more than 2 days before the patient's start of the study.
Item
The initiation of an add-on AED therapy can not be more than 2 days before the patient's start of the study.
boolean
C1704686 (UMLS CUI 2011AA)
C0003299 (UMLS CUI 2011AA)
255632006 (SNOMED CT 2011_0131)
MTHU006781 (LOINC Version 232)
C0039798 (UMLS CUI 2011AA)
C0439090 (UMLS CUI 2011AA)
276137008 (SNOMED CT 2011_0131)
LE (HL7 V3 2006_05)
C0205448 (UMLS CUI 2011AA)
19338005 (SNOMED CT 2011_0131)
C0439228 (UMLS CUI 2011AA)
258703001 (SNOMED CT 2011_0131)
D (HL7 V3 2006_05)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C0030705 (UMLS CUI 2011AA)
116154003 (SNOMED CT 2011_0131)
C2348558 (UMLS CUI 2011AA)
Item Group
Ausschlusskriterien
CL425201 (UMLS CUI 2011AA)
N/A
Item
No Information Available
boolean
C1546437 (UMLS CUI 2011AA)
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