Clinical Trials Logo
  1. Home
  2. Spinal Deformity
  3. NCT04071665

A Modified Lateral Lumbar Interbody Fusion VS. Transforaminal Lumbar Interbody Fusion for Adult Degenerative Scoliosis

Spinal Deformity Clinical Trial

Official title:
A Modified Lateral Lumbar Interbody Fusion VS. Transforaminal Lumbar Interbody Fusion for Adult Degenerative Scoliosis

Clinical Trial Summary

A modified lateral lumbar interbody fusion VS. transforaminal lumbar interbody fusion for the treatment of adult degenerative scoliosis with 2 year follow-up with a multiple center, randomized case-control study

Clinical Trial Description

Adult degenerative scoliosis (ADS) is the most common spinal deformity in the elderly, and the severe patients need surgical treatment. The elderly are often complicated with many medical diseases and the perioperative risk is high, so minimally invasive surgery is a new choice for spinal surgeons to treat ADS. Modified lateral lumbar interbody fusion (CLIF) is an new modified spinal minimally invasive interbody fusion technique in the investigator's department. The results of preliminary studies showed that it has the advantages of less trauma, short operation time and fewer complications, and the clinical and imaging outcome are remarkable. Therefore, the present study aims to establish a multicenter, large sample prospective randomized controlled study to explore the technical advantages and surgical indications of the new technique in the treatment of ADS by comparing with the traditional posterior spinal interbody fusion; (2) to compare the postoperative clinical and imaging results and analyze the surgical complications and preventive measures; (3) to establish a long-term follow-up to further quantify the clinical and imaging outcome of the new technique. Therefore, this study will further verify the safety and effectiveness of the CLIF in the treatment of ADS on the basis of previous studies, and provide a new clinical approach for minimally invasive treatment of ADS. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04071665
Study type Interventional
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Fangcai LI, Ph.D
Phone 86-057187784594
Email 89048991@qq.com
Status Recruiting
Phase N/A
Start date May 1, 2020
Completion date December 31, 2022
View Details
See also
  Status Clinical Trial Phase
Completed NCT01220505 - Post Market Surveillance to Evaluate the Effectiveness the Polaris Deformity Spinal System
Terminated NCT00974623 - Bone Graft Materials Observational Registry N/A
Withdrawn NCT02058238 - ADDRESS - Adult Deformity Robotic vs. Freehand Surgery to Correct Spinal Deformity
Recruiting NCT05323448 - Efficacy of ARISTA-AH for Restoring Hemostasis Following Posterior Long-segment Spinal Fusion. N/A
Recruiting NCT05108948 - Research of Factors Determining the Improvement of Quality of Life at One Year of Adult Patients Treated for Spinal Deformity (COFTASD)
Completed NCT02950532 - Posterior Ligament Complex Assessment Without Magnetic Resonance Image in Thoracolumbar Fractures
Completed NCT01982045 - RCT of AttraX® Putty vs. Autograft in Instrumented Posterolateral Spinal Fusion N/A
Active, not recruiting NCT00738439 - Prospective, Multi-Center Adult Spinal Deformity Outcomes Database Registry
Completed NCT05579834 - Hemothorax Caused by Posterior Correction Surgery for Spinal Deformity
Completed NCT01608854 - Comparison of Antibiotic Protocols in Spine Patients With Postoperative Drains N/A
Active, not recruiting NCT04899297 - Quality of Life in Parents of Adolescents With Spinal Deformities: Development of a New Questionnaire.
Completed NCT05239962 - A Reliability And Validity Study Of The Urdu Version Of Spine Functional Index.
Active, not recruiting NCT05001893 - Clinical Safety and Efficacy of S53P4 Bioactive Glass Putty in Spinal Fusion Surgery
Completed NCT01601054 - Supplemental Anterior Lumbar Interbody Fusion (ALIF) in Spinal Deformity N/A
Active, not recruiting NCT04670536 - The Degen Study: Post-market Clinical Follow-up on the PASS LP, PASS Degen and PASS Tulip Systems (PASS DEGEN)
Completed NCT03880292 - Spinal Deformity Intraoperative Monitoring. N/A
Recruiting NCT05856370 - The Ailliance Post-Market Clinical Study N/A
Recruiting NCT05146193 - AI-Powered Scoliosis Auto-Analysis System Multicenter Development and Validations
Active, not recruiting NCT04642456 - Balance Assessment Scale and Strength Measurement Protocol to Measure Functionality in Adults With Spinal Deformity N/A
Completed NCT06009601 - The Relationship Between Pectus Deformities and Spinal Pathologies