Rod Shape Changing After Scoliosis Correction Surgery
Scoliosis Idiopathic, Scoliosis, Severe
About this trial
This is an interventional treatment trial for Scoliosis Idiopathic focused on measuring scoliosis, posterior segmentdesis, 3D scanning, EOS 2D/3D
Eligibility Criteria
Inclusion Criteria:
- routine patient care of University of Pécs Medical School Department of Orthopaedics
- diagnosed idiopathic adolescent scoliosis
- scoliosis induced surgical indication (Cobb-degree>45)
Exclusion Criteria:
- early onset or adult degenerative scoliosis
- scoliosis with known origin
- the angle of the curve does not reach the criteria of surgical indication (Cobb-degree<45)
- former spine surgery
Sites / Locations
- Ádám Schlégl
Arms of the Study
Arm 1
Experimental
Study group
Patients with scoliosis induced surgical indication (Cobb-degree>45). Posterior screw-rod fixation segmentdesis Before the implantation, right after the implantation and after the in situ bending 3D scanning of the rod using Artec Eva Spider type manual 3D scanner will be performed. Scanning is possible from a more than 60 cm distance, so that means the operational area stays sterile. EOS Micro Dose imaging will be done on the third day after surgery, on the third, the sixth, the twelfth and twenty fourth month after surgery (as in the actual clinical protocal).