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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04671147
Other study ID # IndonesianOrthopaedic
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2016
Est. completion date December 31, 2019

Study information

Verified date December 2020
Source Indonesian Orthopaedic Association
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators collected retrospective data of severe (>80o) and rigid scoliosis patients who underwent preoperative traction before correction surgery from 2016 to 2018. The first group consisted of patients who underwent Cotrel traction exercises and second group underwent continuous-progressively increasing Skull Tongs Femoral Traction (STFT) traction. Posterior fusion was performed in all patients. Intraoperative parameters (blood loss, operation time and level instrumented) and radiologic change (initial, post-traction and postoperative Cobb Angle) was evaluated and analyzed


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date December 31, 2019
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 10 Years to 40 Years
Eligibility Inclusion Criteria: - adolescence/adult idiopathic scoliosis; - severe and rigid scoliosis (defined as Cobb angle more than 80° and flexibility index less than 25%); - either skull tongs-femoral traction or Cotrel longitudinal traction used in the preoperative time period Exclusion Criteria: - other types of scoliosis (neuromuscular scoliosis, congenital scoliosis, etc.) - intradural abnormalities (diastomatomyelia, tethered cord, etc) - history of previous spine surgery

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Preoperative traction
Compare two methods of preoperative traction (Cotrel traction exercises and skull tongs femoral traction)

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Indonesian Orthopaedic Association

Outcome

Type Measure Description Time frame Safety issue
Primary Radiologic change Preoperative, post traction and postoperative xray - Baseline - Immediately after 2 weeks of preoperative traction - immediately after the correction surgery
Secondary Blood loss The amount of blood loss during the correction surgery Intraoperative
Secondary Duration of surgery The time required to perform the correction surgery Intraoperative
Secondary Number of instrumented levels the number of vertebrae instrumented during the correction surgery Intraoperative
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