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Scoliosis Neuromuscular clinical trials

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NCT ID: NCT03611244 Recruiting - Clinical trials for Duchenne Muscular Dystrophy

Prevention of Scoliosis in Patients With Duchenne Muscular Dystrophy Using Portable Seat Device

Start date: August 7, 2018
Phase: N/A
Study type: Interventional

This study will be conducted without blind method. The portable seat device devised to maintain lumbar lordosis will be made within 1 year after the loss of ambulation in the participants with Duchenne muscular dystrophy with prospective design. In the control group, the presence of scoliosis will be calculated 5 years after the loss of ambulation in participants with Duchenne muscular dystrophy through analysis of retrospective medical records who had not been applied the portable seat device.