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Post Polio Syndrome, PPS clinical trials

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NCT ID: NCT00160082 Completed - Clinical trials for Post Polio Syndrome, PPS

Efficacy and Safety of Xepol (Human Immunoglobulin) in Subjects With Post-Polio Syndrome (PPS)

Start date: January 2001
Phase: N/A
Study type: Interventional

The primary objective was to assess the effect of Xepol compared to placebo on physical health and on muscle strength in subjects with post-polio syndrome.The secondary objective was to assess the effect of Xepol compared to placebo on functional balance, activity patterns, pain, fatigue, sleep, vitality, muscular strength, pulmonary capacity, walking ability, balance and safety.