A Feasibility Study on the use of Percutaneous Instrumentation for less invasive surgery of Scoliosis Deformity in Children with Neuromuscular Disease.

A Feasibility Study on the use of Percutaneous Instrumentation for less invasive surgery of Scoliosis Deformity in Children with Neuromuscular Disease. - LISCOS (Less Invasive Scoliosis Surgery)

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON33242

Enrollment

Registered

2009-12-23

Start date

2010-09-09

Completion date

Unknown

Last updated

2024-05-06

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

Conditions

acquired spine deformity scoliose

Interventions

All children and adolescents will be treated with the percutaneous less invasive scoliosis correction. A group of 5 children will be studied first to observe any surgical adverse events or postopera

Eligibility

Age

12 Years to 17 Years

Inclusion criteria

Inclusion criteria: age > 12 yrs

Exclusion criteria

Exclusion criteria: age > or = 18 yrs previous spine surgery stiff scoliosis deformity with little chance for closed reduction (spastic children)

Design outcomes

Primary

Measure	Time frame
The technical feasibility to correct a neuromuscular scoliosis and to maintain the correction using the experimental less invasive pecutaneous system.	—

Secondary

Measure	Time frame
The amount of blood loss, ICU stay (days), postoperative complications and the amount of pain.	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)