Informatie:
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ID
30933
Beschrijving
Levetiracetam in Central Pain in Multiple Sclerosis(MS); ODM derived from: https://clinicaltrials.gov/show/NCT00423527
Link
https://clinicaltrials.gov/show/NCT00423527
Trefwoorden
Versies (1)
- 04-07-18 04-07-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
4 juli 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Multiple Sclerosis NCT00423527
Eligibility Multiple Sclerosis NCT00423527
- StudyEvent: Eligibility
Similar models
Eligibility Multiple Sclerosis NCT00423527
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
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])
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])
C1504479 (UMLS CUI [1,2])
Cause Pain
Item
other cause of pain
boolean
C0015127 (UMLS CUI [1,1])
C0030193 (UMLS CUI [1,2])
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])
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])
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])
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])
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])
C0003286 (UMLS CUI [2])
C0242402 (UMLS CUI [3])