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Clinical Trials/NCT04415814
NCT04415814UnknownNot Applicable

Unilateral Versus Bilateral Pedicle Screw Fixation for Lumbar Degenerative Diseases

I.M. Sechenov First Moscow State Medical University1 site in 1 country40 target enrollmentStarted: January 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
40
Locations
1
Primary Endpoint
fusion rate of the operated spine segment

Study Overview

Brief 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.

Detailed 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Written informed consent of the patient to participate in the study;
  • •Patients with degenerative diseases of the lumbar spine.
  • •The opportunity for observation during the entire study period (12 months);
  • •Mental adequacy, ability, willingness to cooperate and follow the doctor's recommendations.

Exclusion Criteria

  • •The refusal of a patient from surgery
  • •The presence of contraindications to surgery
  • •Severe forms of diabetes (glycosylated hemoglobin >9%);
  • •Blood diseases (thrombopenia, thrombocytopenia, anemia with Hb< 90g\l);
  • •The unwillingness of the patient to conscious cooperation.

Arms & Interventions

Group 1 (Unilateral Pedicle Screw Fixation)

Experimental

Patients will undergo stabilizing surgery on the lumbar spine for degenerative diseases of the spine. Pedicular screws will be installed unilaterally, which means on one side of the spinous processes. The system will be fixed with standard rod and blockers.

Intervention: Unilateral Pedicle Screw Fixation (Procedure)

Group 2 (Bilateral Pedicle Screw Fixation)

Active Comparator

Patients will undergo stabilizing surgery on the lumbar spine for degenerative diseases of the spine. Pedicular screws will be installed bilaterally, which means on the both sides of the spinous processes. The system will be fixed with standard rods and blockers.

Intervention: Bilateral Pedicle Screw Fixation (Procedure)

Outcomes

Primary Outcomes

fusion rate of the operated spine segment

Time Frame: in 12 months after surgery

Control CT/Radiography examination

fusion rate of the operated spine segment

Time Frame: in 3 months after surgery

Control CT/Radiography examination

fusion rate of the operated spine segment

Time Frame: in 6 months after surgery

Control CT/Radiography examination

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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