ID

30933

Description

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

Link

https://clinicaltrials.gov/show/NCT00423527

Keywords

Versions (1)
  1. 7/4/18 7/4/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

July 4, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Multiple Sclerosis NCT00423527

English

Eligibility Multiple Sclerosis NCT00423527

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
ms diagnosis verified
Description

Multiple Sclerosis

Data type

boolean

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

Age

Data type

boolean

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

Central pain Symptoms Duration

Data type

boolean

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

Central pain Neurologic Examination

Data type

boolean

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

Childbearing Potential Contraceptive methods

Data type

boolean

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

Informed Consent

Data type

boolean

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

Pain Pain scale

Data type

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
other cause of pain
Description

Cause Pain

Data type

boolean

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

Allergic Reaction Levetiracetam

Data type

boolean

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

Adverse reaction to drug Levetiracetam

Data type

boolean

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

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
severe disease
Description

Disease Severe

Data type

boolean

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

Protocol Compliance Unable

Data type

boolean

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

Antidepressive Agents | Anticonvulsants | Opioids

Data type

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 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
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