Tokyo, Dec. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059903) titled 'Safety and efficacy of home-based neuromuscular electrical stimulation device in patients with Charcot-Marie-Tooth disease: a randomized controlled crossover trial' on Dec. 1.
Study Type:
Interventional
Study Design:
Basic Design - Cross-over
Randomization - Randomized
Blinding - Open -no one is blinded
Control - No treatment
Primary Sponsor:
Institute - Kyoto prefectural university of medicine
Condition:
Condition - Charcot-Marie-Tooth disease
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To evaluate the efficacy and safety of the NMES device "FootFit" (MTG Co....