Skip to content

Postoperative Pain in Adolescent Idiopathic Scoliosis Surgery

Evaluation of Surgical Methods in Terms of Postoperative Pain in Adolescent Idiopathic Scoliosis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04822935
Enrollment
31
Registered
2021-03-30
Start date
2021-06-30
Completion date
2021-11-17
Last updated
2021-11-19

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

Conditions

Scoliosis; Adolescence

Brief summary

Scoliosis is a 3-dimensional, structural deformity of the spine. Idiopathic scoliosis is the most common type and it constitutes 75-80% of all scoliosis. Surgical methods are the most effective way to correct the deformity in patients who cannot achieve adequate improvement with supportive therapy. Adolescent idiopathic scoliosis surgeries are among the most invasive surgeries performed on children and adolescents. Large surgical incision and massive tissue damage cause severe postoperative pain. In this study, we aim to compare posterior instrumentation (PE) and vertebral body tethering (VBT) surgeries performed in adolescent idiopathic scoliosis patients in terms of anesthetic management and postoperative pain.

Interventions

PROCEDUREVertebral Body Tethering

VBT surgery is a surgery performed by thoracotomy in adolescent idiopathic scoliosis patients.

Sponsors

Istanbul University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
9 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* ASA score 1-3 patients * Adolescent idiopathic scoliosis patients * Patients who accepted to be included in the study and received written parental consent

Exclusion criteria

* Patients with vertebral anomaly due to a secondary reason * Patients with a diagnosed syndrome * Patients with a Cobb angle below 40. * Patients who undergoing reoperation

Design outcomes

Primary

MeasureTime frameDescription
Comparison in terms of postoperative pain48 hoursOpioid consumption and VAS (visual analog scale) (0: no pain, 10: the worst pain imaginable) for measurement of postoperative pain

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026