Lumbar Disc Disease Clinical Trial
Official title:
Intra-operatory Neurophysiological Monitoring Changes as a Predictive Clinical Outcome Measure in Radiculopathy Associated to Lumbar Disk Disease. Two Years Follow-up
The purpose of this study is to determine the relation among: (1) changes in voltage and
amplitude of trans-operatory records obtained through the use of Intra-operative
Neurophysiological Monitoring (IONM), and (2) clinical outcomes; of patients who underwent 1
or 2 levels surgical decompression at lumbar spine.
IONM is the use of real time neurophysiological techniques during spinal surgeries. The
modalities included in this study are:
- Somatosensory evoked potentials (SSEPs).
- Trans-cranial electric motor evoked potentials (tceMEPs).
- Spontaneous electromyography (EMG).
Clinical outcome of the patients will be assessed through a careful evaluation of clinical
data, as well as the application of three outcome scales:
- Oswestry Disability Index 2.1a
- Visual Analogue Scale for Pain
- Patient's Overall Impression of Change
Radiculopathy associated to lumbar disk disease is one of the most common reasons for a
spine surgeon to be consulted. The pathophysiology of degenerative spine disease is
acknowledged as complex, involving a wide array of risk factors ranging from genetic
polymorphisms, to behavioural characteristics. While conflicting opinions exist with regard
the direction of treatment for lumbar disk disease, de-compressive surgery is currently the
gold standard for patients in which protocols of physiotherapy and analgesics have failed to
comply.
Intraoperative neurophysiological monitoring (IONM) is widely used in the practice of spine
surgery as a mean of preventing and reducing severe complications inherent to surgical
techniques like paraparesis, paraplegia and quadriplegia. Indeed, a great deal of funding
and work have been devoted to research projects seeking to determine the impact of IONM in
reducing these risks. The results of such projects have been notoriously interesting, and
frequently opposing to each other. This has lead to an open debate on weather the use of
IONM may or not be justified by better outcomes in patients who undergo such procedure. To
our knowledge there is no study in the literature that has addressed the potential role of
the IOM to predict the long-term outcome of the patient in therms of radicular symptoms
improvement.
;
Observational Model: Case-Only, Time Perspective: Retrospective
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01941563 -
A Study of SI-6603 in Patients With Lumbar Disc Herniation
|
Phase 3 | |
Completed |
NCT04061759 -
Physiotherapy in Lumbar Disc Pathologies
|
N/A | |
Recruiting |
NCT04727385 -
Intervertebral DXM Gel Injection in Adults With Painful Lumbar Degenerative Disc Disease
|
N/A | |
Completed |
NCT04587401 -
The Effects of Anesthesia on Cerebral Perfusion in Patients With High Blood Pressure
|
N/A | |
Not yet recruiting |
NCT06034041 -
The Effect of Mediclore as an Anti-adhesion Agent and Safety in Full-endoscopic Spine Surgery: a Preliminary Study
|
Phase 4 | |
Recruiting |
NCT04134975 -
Evaluation of the Contribution of Intraoperative Scans Coupled With the Navigation for the Precision of the Positioning of the Pedicle Screws During a Lumbar Spine Surgery: a Prospective Randomised Study
|
N/A | |
Recruiting |
NCT05146583 -
Injection of Autologous Bone Marrow Aspirate in Patients With Degenerative Disc Disease.
|
||
Recruiting |
NCT04641039 -
Postoperative Scar in the Control Excess of Mobility Induced by Annulus Removal on Inserting a Lumbar Disc Prosthesis
|
N/A | |
Completed |
NCT04301232 -
Fast-Track Eligibility and Hospital Discharge for Outpatient Lumbar Discectomy
|
||
Recruiting |
NCT06154005 -
OsteoAdapt SP Advanced Bone Graft Feasibility Study - Transforaminal Interbody Lumbar Fusion
|
Phase 1/Phase 2 | |
Completed |
NCT03977961 -
The Six-Minute Walking Test (6MWT) as a Measure of Functional Impairment in Lumbar Degenerate Disc Disease.
|
||
Enrolling by invitation |
NCT05444751 -
GA + ESP vs. SA + ESP in Lumbar Decompression Surgeries
|
Phase 3 | |
Completed |
NCT02700451 -
Post-op Acetaminophen vs NSAID Use on Lumbar Spinal Fusion Outcomes
|
N/A | |
Completed |
NCT02421601 -
A Study of SI-6603 in Patients With Lumbar Disc Herniation
|
Phase 3 | |
Active, not recruiting |
NCT03733626 -
Clinical Outcomes Associated With the Use of ViviGen® for the Treatment of Lumbar Degenerative Disc Disease
|
N/A | |
Recruiting |
NCT04042844 -
A Single Dose of BRTX 100 for Patients With Chronic Lumbar Disc Disease (cLDD)
|
Phase 2 | |
Recruiting |
NCT06462729 -
LDGraft in Single Level Anterior Lumbar Interbody Fusion (ALIF)
|
Phase 1/Phase 2 | |
Completed |
NCT05345249 -
Erector Spinae Plane Block as Pain Management After Lumbar Fusion Surgery
|
Phase 4 | |
Active, not recruiting |
NCT03060434 -
Pentoxifylline and Lumbar Radiculopathy
|
Phase 4 | |
Withdrawn |
NCT02852187 -
Single Center Study Comparing MOBIS II ST vs MOBIS PEEK
|
N/A |