Contributors | p. xi |
Preface to first edition | p. xix |
Preface to second edition | p. xxi |
Acknowledgements | p. xxiii |
Introduction | |
Aspects of multiple sclerosis that relate to clinical trial design and treatment | p. 3 |
Clinical trial methodology | |
Measures of neurologic impairment and disability in multiple sclerosis | p. 23 |
Assessment of neuropsychological function in multiple sclerosis | p. 37 |
Health-related quality of life assessment in multiple sclerosis | p. 61 |
Magnetic resonance imaging in multiple sclerosis: an overview | p. 81 |
Measures of gadolinium enhancement in multiple sclerosis | p. 97 |
Measures of magnetization transfer in multiple sclerosis | p. 125 |
Measures of T1 and T2 relaxation in multiple sclerosis | p. 155 |
Measurement of central nervous system atrophy in multiple sclerosis | p. 173 |
Measures to quantify axonal damage in vivo based on magnetic resonance spectroscopy in multiple sclerosis | p. 193 |
Functional imaging in multiple sclerosis | p. 207 |
Use of cost analyses to improve our understanding of the therapeutic trade-offs for multiple sclerosis | p. 221 |
Ethical considerations in multiple sclerosis clinical trials | p. 231 |
The process of drug development and approval in the USA, the European Union and Canada | p. 241 |
Sponsors, monitoring committees and investigators: the investigator's perspective | p. 257 |
Guidelines for clinical trials of new therapeutic agents in multiple sclerosis: reporting extended results from phase III clinical trials | p. 261 |
The failed clinical trial in multiple sclerosis | p. 267 |
The challenge of long-term studies in multiple sclerosis: use of pooled data, historical controls, and observational studies to determine efficacy | p. 277 |
Emerging concepts of pathogenesis: relationship to MS therapies | p. 289 |
Clinical trials of disease-modifying therapy | |
Interferons in relapsing-remitting multiple sclerosis | p. 325 |
Interferons in secondary progressive multiple sclerosis | p. 347 |
Biological responses to type I interferons: relationship to therapeutic effects in multiple sclerosis | p. 363 |
Glatiramer acetate as therapy for multiple sclerosis | p. 379 |
Use of mitoxantrone to treat multiple sclerosis | p. 403 |
Intravenous immunoglobulin to treat multiple sclerosis | p. 427 |
Therapeutic plasma exchange for multiple sclerosis | p. 445 |
Treatment of multiple sclerosis with methylprednisolone | p. 461 |
Cyclophosphamide treatment of multiple sclerosis | p. 483 |
Treatment of multiple sclerosis by hematopoietic stem cell transplantation | p. 501 |
Emerging disease-modifying therapies for multiple sclerosis | p. 515 |
Combination therapies in multiple sclerosis | p. 523 |
Sex hormones and other pregnancy-related factors with therapeutic potential in multiple sclerosis | p. 535 |
Complementary and alternative treatments in multiple sclerosis | p. 551 |
Disease-modifying drug therapy in clinical practice | |
Disease-modifying drug therapy for multiple sclerosis in clinical practice | p. 567 |
Treatment for patients with primary progressive multiple sclerosis | p. 589 |
Fatigue in multiple sclerosis | p. 599 |
Management of spasticity in multiple sclerosis | p. 609 |
Management of bladder and sexual dysfunction in multiple sclerosis | p. 621 |
Treatment of disorders of mood and affect in multiple sclerosis | p. 651 |
Treatment of pain, paresthesias, and paroxysmal disorders in multiple sclerosis | p. 689 |
Treatment of tremor caused by multiple sclerosis | p. 705 |
Management of cognitive impairment in multiple sclerosis | p. 715 |
Rehabilitation in multiple sclerosis patients | p. 729 |
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