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Completed

NCT Number: NCT03863496

Efficacy of Surgical Treatment by Different Pedicle Screw Systems in Pediatric Neuromuscular Spinal Deformity

This study was sponsored by Federal state budgetary institution "Russian scientific center for traumatology and orthopedics" n.a. acad. G.A. Ilizarov" of the Ministry of Health of Russian Federation. The study will take place at this center.

It is expected to enroll 70 patients aged 6-25 years with NMD, all of whom will be subjected to thoracic and lumbar spinal deformity surgery.

Patients will be divided into two groups depending on skeletal maturity. The degree of skeletal maturity will be determined on the basis of an X-ray study of spinal and pelvic bones. The type of surgical correction will depend on the group.

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Key information

Age range

6 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ilizarov

Kurgan, 640014, Russia

About this study

First group of patients: local dorsal access. Cranial access: at the level of posterior Th2 5 structures and caudally at the level of L4-S2 vertebrae with exposure of posterior upper spines of iliac wings. Skeletization of vertebrae will be done within transverse processes. Pedicle support points are set bilaterally cranially at each segment level for the space of 3 segments. Caudal support base is formed with pedicle screws in lateral masses of the sacral bone or iliac crests at the level of L5-S1 vertebrae. Control fluorography is performed in two standard planes in order to control screw position. Two "dynamic" rods are formed on the basis of the distance between screw heads allowing 2 cm for distraction; these are two rods connected with a longitudinal connector and bent following the normal sagittal spine profile. After that, channels are formed on both sides under m. erector spinae in the cranial/caudal direction. Pre-bent rods with connectors are placed into the prepared channels. The metal construct is stabilized with internal set screws. If necessary, the construct may be stiffened with crosslinks. Control fluorography is performed in two standard planes in order to control implant position and evaluate correction. The intervention completes with local dorsal spinal fusion with an autobone at the level of base screws. The wound is sewn up in layers tightly.

Group two: dorsal access to the posterior column is gained in accordance with the preoperative plan. The access length depends on the instrumentation area. Vertebral skeletization is performed within transverse processes. Subgroup 1 - pedicle support points are set bilaterally at each segment level. Subgroup 2 - pedicle support points are set bilaterally in every second segment. Segmented instrumentation of 3 cranial segments to prevent dislocation of metal construct elements at the level of Th2-4 or Th3-5 vertebrae is a special measure. Similar to group I, caudal support base is formed with pedicle screws in lateral masses of the sacral bone or iliac crests at the level of L5-S1 vertebrae. Control fluorography is performed after that in two standard planes in order to control screw position. Segmented facetectomy is recommended for additional spine mobilization. Pre-bent rods are placed into support points. Deformity correction is performed by means of a translational maneuver, segmented distraction (concave side) and compression (convex side). The metal construct is stabilized with internal set screws. If necessary, the construct may be stiffened with crosslinks. Control fluorography is performed in two standard planes in order to control implant position and evaluate correction. The intervention completes with dorsal spinal fusion with an autobone along the implants. The postoperative bed is subjected to Redon drain. The drainage is exteriorized to the skin via a separate puncture. The wound is sewn up in layers tightly.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed and dated informed consent for participation in the study (separate informed consents for child and parents/caregivers), obtained before conducting any study procedures
  • Verified and documented diagnosis (neuromuscular desease, NMD) with the results of neurologic examination
  • Deformity of thoracic and/or lumbar spine associated with NMD, which requires surgical intervention

Exclusion criteria

  • Patient unwillingness or inability to follow study procedures
  • Absence of signed and dated informed consent for participation in the study (as for child and for parents/caregivers)
  • Patient participation in another clinical study, which can influence the results of this study
  • Life expectancy <12 months
  • Concomitant diseases, which preclude patient participation in this study according to doctor's opinion

Treatment and study plan

Scoliosis surgery

Procedure

All patients will be implanted Medtronic CD Horizon Legacy 4.5 and 5.5 under X-ray control (C-arm), intraoperative spinal deformity surgery safety control and standard anesthetic support.

Primary outcomes

  1. First Scoliotic Curve

    Time frame: before surgery

    First scoliotic curve before surgery in Cobb degrees

  2. Second Scoliotic Curve

    Time frame: before surgery

    Second scoliotic curve before surgery in Cobb degrees

  3. Tilt of the Pelvis Relative to the Horizon

    Time frame: before surgery

    tilt of the pelvis relative to the horizon before surgery in Cobb degrees

  4. Kyphotic Curve Th5-Th12

    Time frame: before surgery

    Kyphotic curve Th5-Th12 before surgery in Cobb degrees

  5. Lordotic Curve L1-S1

    Time frame: before surgery

    Lordotic curve L1-S1 before surgery in Cobb degrees

Secondary outcomes

  1. First Scoliosis Curve

    Time frame: 10 days after surgery

    First scoliotic curve after surgery in Cobb degrees

  2. Second Scoliotic Curve

    Time frame: 10 days after surgery

    Second scoliotic curve after surgery in Cobb degrees

  3. Tilt of the Pelvis Relative to the Horizon

    Time frame: 10 days after surgery

    tilt of the pelvis relative to the horizon after surgery in Cobb degrees

  4. Kyphotic Curve Th5-Th12

    Time frame: 10 days after surgery

    Kyphotic curve Th5-Th12 after surgery in Cobb degrees

  5. Lordotic Curve L1-S1

    Time frame: 10 days after surgery

    Lordotic curve L1-S1 after surgery in Cobb degrees

Sponsors and collaborators

Lead sponsor

Ilizarov Center

Other

Collaborators

  • Medtronic

Registry information

Important dates

Study start
2018
Primary completion
2021
Study completion
2021
First posted
Mar 5, 2019
Registry last updated
Jun 10, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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