ID

30933

Descripción

Levetiracetam in Central Pain in Multiple Sclerosis(MS); ODM derived from: https://clinicaltrials.gov/show/NCT00423527

Link

https://clinicaltrials.gov/show/NCT00423527

Palabras clave

Versiones (1)
  1. 4/7/18 4/7/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

4 de julio de 2018

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Multiple Sclerosis NCT00423527

Inglés

Eligibility Multiple Sclerosis NCT00423527

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
ms diagnosis verified
Descripción

Multiple Sclerosis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0026769
age > 18 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
central pain symptoms for more than 3 months
Descripción

Central pain Symptoms Duration

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0234243
UMLS CUI [1,2]
C1457887
UMLS CUI [1,3]
C0449238
central pain diagnosis confirmed by neurological examination
Descripción

Central pain Neurologic Examination

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0234243
UMLS CUI [1,2]
C0027853
adequate anticonceptive treatment for women with child bearing potential
Descripción

Childbearing Potential Contraceptive methods

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
baseline pain of more than 4 on numeric rating scale
Descripción

Pain Pain scale

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C1504479
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
other cause of pain
Descripción

Cause Pain

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0015127
UMLS CUI [1,2]
C0030193
previous allergic reaction towards levetiracetam
Descripción

Allergic Reaction Levetiracetam

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1527304
UMLS CUI [1,2]
C0377265
known adverse drug reaction on levetiracetam
Descripción

Adverse reaction to drug Levetiracetam

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0041755
UMLS CUI [1,2]
C0377265
pregnancy
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
severe disease
Descripción

Disease Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0205082
inability to follow study protocol
Descripción

Protocol Compliance Unable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C1299582
treatment with antidepressants, other anticonvulsants or opioids
Descripción

Antidepressive Agents | Anticonvulsants | Opioids

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003289
UMLS CUI [2]
C0003286
UMLS CUI [3]
C0242402
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Similar models

Eligibility Multiple Sclerosis NCT00423527

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Multiple Sclerosis
Item
ms diagnosis verified
boolean
C0026769 (UMLS CUI [1])
Age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
Central pain Symptoms Duration
Item
central pain symptoms for more than 3 months
boolean
C0234243 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Central pain Neurologic Examination
Item
central pain diagnosis confirmed by neurological examination
boolean
C0234243 (UMLS CUI [1,1])
C0027853 (UMLS CUI [1,2])
Childbearing Potential Contraceptive methods
Item
adequate anticonceptive treatment for women with child bearing potential
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Informed Consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Pain Pain scale
Item
baseline pain of more than 4 on numeric rating scale
boolean
C0030193 (UMLS CUI [1,1])
C1504479 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Cause Pain
Item
other cause of pain
boolean
C0015127 (UMLS CUI [1,1])
C0030193 (UMLS CUI [1,2])
Allergic Reaction Levetiracetam
Item
previous allergic reaction towards levetiracetam
boolean
C1527304 (UMLS CUI [1,1])
C0377265 (UMLS CUI [1,2])
Adverse reaction to drug Levetiracetam
Item
known adverse drug reaction on levetiracetam
boolean
C0041755 (UMLS CUI [1,1])
C0377265 (UMLS CUI [1,2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Disease Severe
Item
severe disease
boolean
C0012634 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Protocol Compliance Unable
Item
inability to follow study protocol
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Antidepressive Agents | Anticonvulsants | Opioids
Item
treatment with antidepressants, other anticonvulsants or opioids
boolean
C0003289 (UMLS CUI [1])
C0003286 (UMLS CUI [2])
C0242402 (UMLS CUI [3])
Volver a la parte superior de la página 

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