Unilateral Versus Bilateral Pedicle Screw Fixation for Lumbar Degenerative Diseases

Fusion of Spine Clinical Trial

Official title: Unilateral Versus Bilateral Pedicle Screw Fixation for Lumbar Degenerative Diseases

Status Recruiting

Clinical Trial Summary

Determining the treatment strategy for patients with degenerative diseases of the spine is extremely difficult, without an accurate understanding of the nature of stress distribution in the vertebral-motor segments of the spine, as well as biomechanical changes that are associated with degenerative diseases of the spine. In this clinical study, we want to compare the use of unilateral and bilateral transpedicular fixation for treating the patients with degenerative diseases of the lumbar spine.

Clinical Trial Description

It is planned to use posterior stabilization without interbody fusion. In the postoperative period, all the patients receive antibacterial and analgesic therapy. The early postoperative period is spent in a hospital. Repeated appearances for control examinations (3, 6, 12 months) are provided for physical examination (EQ-5D, Oswestry Disability Index) and performing radiographs or computed tomography (CT) of the spine. All patients undergo a standard rehabilitation course. ;

Related Conditions & MeSH terms

• Fusion of Spine

• NCT number: NCT04415814
• Study type: Interventional
• Source: I.M. Sechenov First Moscow State Medical University
• Contact: Vadim Cherepanov, MD, PhD
• Phone: +79166548850
• Email: cvg_cherepanov@mail.ru
• Status: Recruiting
• Phase: N/A
• Start date: January 1, 2019
• Completion date: August 31, 2022