A Feasibility Study on the use of Percutaneous Instrumentation for less invasive surgery of Scoliosis Deformity in Children with Neuromuscular Disease.
Completed
- Conditions
- acquired spine deformityscoliose1000595910005944
- Registration Number
- NL-OMON33242
- Lead Sponsor
- niversitair Medisch Centrum Utrecht
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 10
Inclusion Criteria
age > 12 yrs < 18 yrs
neuromuscular disease or spina bifida with scoliosis deformity
scoliosis deformity that needs operative treatment
Exclusion Criteria
age > or = 18 yrs
previous spine surgery
stiff scoliosis deformity with little chance for closed reduction (spastic children)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The technical feasibility to correct a neuromuscular scoliosis and to maintain<br /><br>the correction using the experimental less invasive pecutaneous system. </p><br>
- Secondary Outcome Measures
Name Time Method <p>The amount of blood loss, ICU stay (days), postoperative complications and the<br /><br>amount of pain. </p><br>