Design | Parallel | Modified cross over | Parallel |
Patients included | 67 | 10 | 55 |
Primary outcome | Targeted neurological deficit | Central conduction velocity | Change in log MAR scores |
Secondary outcome | EDSS, FS, FIM, 9HPT, BBT | EDSS, SNRS, time to walk 20 m, manual muscle testing | EDSS, AI, FS, VER, visual fields, visual acuity, measures of disease activity |
Dosage/time | 0.4 g/kg for 5 days, then every 2 weeks for 3 months (total 11 infusions), evaluation after 6 months | 0.4 g/kg for 5 days (total 5 infusions), evaluation 6 weeks later | 0.4 g/kg for 5 days, then every 4 weeks for 3 months (total 8 infusions), evaluation after 6 months |