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Prevention of scoliosis using portable seat device devised to maintain lumbar lordosis

Prevention of scoliosis in patients with Duchenne muscular dystrophy using portable seat device devised to maintain lumbar lordosis : 5 year follow up study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0003036
Enrollment
98
Registered
2018-07-27
Start date
2018-08-21
Completion date
Unknown
Last updated
2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : Device: portable seat device devised to maintain lumbar lordosis The posterior lumbar spine pads are used to maintain lumbar lordosis and fix it with the shoulder strap so that the

Sponsors

Seoul National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Patients with the diagnosis of Duchenne muscular dystrophy diagnosed by genetic study were included. 1. Within 1 year after loss of ambulation (Vignos scale 7 points or more) 2. If the point at loss of ambulation is 7 years old or older but not more than 15 years old 3. condition without scoliosis at the time of enrollment 4. conditions that do not have physical (eg, cerebral palsy) and mental (eg, moderate or higher intellectual disability) comorbid conditions that will affect the use of postural seat device.

Exclusion criteria

Exclusion criteria: 1. Patients who do not agree to participate in this study 2. Patients not taking steroids 3. Patient with scoliosis

Design outcomes

Secondary

MeasureTime frame
Cobb's angle on spine x-ray on supine position

Primary

MeasureTime frame
Incidence of scoliosis (Frequency of scoliosis more than 10 degrees of Cobb's angle on spine x-ray on supine position)

Countries

Korea, Republic of

Contacts

Public ContactYou Gyoung Yi

Seoul National University Hospital

lyk861124@gmail.com+82-2-2072-0211

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026