Clinical Trials Logo

Clinical Trial Summary

The present study is planned to demonstrate the efficacy and safety of a new pedicle screw system for the specific indication of isthmic spondylolisthesis, as this condition concerns relatively young patients requiring good fixation of the performed reposition to come to satisfactory clinical results.


Clinical Trial Description

Adult Isthmic spondylolisthesis, which is associated with "spondylolysis," is defined as an osseous discontinuity of the vertebral arch at the isthmus (the pars interarticularis), which usually occurs in the fifth lumbar vertebra. The prevalence of isthmic spondylosis is proposed to be about 6% to 26% in different studies. The European Spine Tango registry found 15%. It is proposed to affect more men than women. Conservative treatments including braces, physical therapy, and medication are shown to be effective for some patients; however, surgical treatments are mainly the final effective treatment. There are several different options for surgery among which posterolateral fusion (PLF) is considered as the method of choice. It is shown that PLF is more effective than conservative treatments such as exercise. The fusion helps to fix the motion of the affected segment and therefore, might lead to pain reduction. Decompression, supplemental instrumentation, and supplemental anterior column support are also considered for treatment. These treatment strategies can be used separately or in any combination; however, studies trying to compare separate treatments with a combination of them have led to inconsistent results.

Supplementary pedicle screws might be added to fusion methods for fixation and it is proposed that they have the ability to correct the deformity, reduce the listhesis, and increase the fusion rates, although a majority of the studies comparing instrumented PLF and noninstrumented PLF could not show the superiority of instrumented approaches. The literature has been reviewed in 2000 already, and the method has already been proved to be "practical, safe, and effective" for various spinal indications. Other authors found a better result for isthmic spondylolisthesis patients with posterior lumbar interbody Fusion (PLIF), vs. PLF, especially for high grade isthmic spondylolisthesis.

The present study is planned to demonstrate the efficacy and safety of a new pedicle screw system for the specific indication of isthmic spondylolisthesis, as this condition concerns relatively young patients requiring good fixation also in the long-term. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03507881
Study type Observational
Source Aesculap AG
Contact
Status Terminated
Phase
Start date July 31, 2018
Completion date January 18, 2019

See also
  Status Clinical Trial Phase
Recruiting NCT04095624 - Does Preoperative Pain Medication Management Influence Surgical Outcomes in Spinal Fusion N/A
Recruiting NCT05367609 - Personalized Perioperative Analgesia Platform (PPAP) for Pediatric Spine Fusion Surgery (sIRB) N/A
Terminated NCT03426137 - Relieving Acute Pain (RAP) Study: A Pilot Study Phase 2
Active, not recruiting NCT04629807 - Anterior Gen Plus Study N/A
Active, not recruiting NCT04379921 - Improving Spine Surgical Care With Real-Time Objective Patient Tracking Using the Apple Watch N/A
Completed NCT02280187 - InductOs® in Real World Spine Surgery; A Retrospective, French, Multi-centric, Study N/A
Not yet recruiting NCT06059820 - Effectiveness of Conservative Treatment in Patients With Thoracic and Lumbar Fractures Without Neurological Deficit
Completed NCT06082245 - TLIP Block and ESP Block For Perioperative Analgesia In Patients With Lumbar Spine Fusion Surgery N/A
Recruiting NCT06102681 - Examination of the Effect of Early Mobilization on Postoperative Recovery, Pain, Quality of Life and Complication Development in Elective Minimally Invasive Spine Surgery N/A
Active, not recruiting NCT05001893 - Clinical Safety and Efficacy of S53P4 Bioactive Glass Putty in Spinal Fusion Surgery
Completed NCT04711668 - Effect of Introperative Ketamine and Lidocaine Infusion on Postoperative Opioid Consumption in Posterior Spinal Fusion Surgery N/A
Not yet recruiting NCT05850468 - Effectiveness of Combining Erector Spinea Block With Non Opioid Infusions as Opioid Free Anesthesia in Spine Surgeries. N/A
Completed NCT04682418 - Pedicle Screw Placement With XVS N/A
Not yet recruiting NCT04679844 - Post Marketing Study of MagnetOs Putty Compared to Demineralized Bone Matrix (DBM) Mixed With Autograft in Patients Undergoing Posterolateral Lumbar Fusion N/A
Not yet recruiting NCT04568837 - Steroids After Spine Fusion Surgery Phase 4
Completed NCT05401526 - Fluid Responsiveness in Prone Position
Not yet recruiting NCT05037968 - MagnetOs Flex Matrix Compared to Cell Based Allografts in Patients Undergoing up to Four-level Instrumented Posterolateral Fusion N/A
Not yet recruiting NCT05691062 - Titanium vs. PEEK Fusion Devices in 1 Level TLIF Phase 4
Recruiting NCT04839783 - Single Position Spine Surgery Registry
Completed NCT05415657 - Denosumab Effect on Bone Quality and Function After Lumbar Fusion Surgery N/A