None listed
Conditions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.The diagnoses multiple sclerosis verified by neurologist 2.age over 18 years 3.neuropathic pain which for at least 3 months and had its onset at least 6 months after the diagnoses multiple sclerosis had been verified 4.average baseline pain score of at least 4 on a 0 to 10 numeric rating scale 5.informed consent Are the trial subjects under 18? Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range
Exclusion criteria
Exclusion criteria: 1.additional cause of pain 2.allergic reactions towards levettiracetam 3.pregnancy or beast feeding period 4.severe illness 5.lack of ability to follow study protocol 6.treatment with antidepressants, anticonvulsants or opioids
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: To determine if levetiracetam will relieve central neuropathic pain in multiple sclerosis ;Secondary Objective: In patients with central neuropathic pain in multiple sclerosis to determine the effect of levetiracetam 1- specific pain symptoms 2-on quality of life 3-pain related sleep disturbance 4-on spasticity ;Primary end point(s): Patients verbal score of pain relief (complete, good, moderate, slight, no, worse) at the end of each treatment period | — |
Countries
Denmark