Degenerative Spondylolisthesis Clinical Trial
Official title:
Multimodal Perioperative Pain Management of Circumferential Lumbar Fusion Improves Recovery
Convalescence after lumbar fusion is dependent on pain. In orthopaedic and abdominal surgery
accelerated stay programs with optimized pain management enhance recovery.
The objective is to evaluate the effect of a revised and optimized perioperative fast track
program in lumbar fusion surgery.
Major spine surgery is usually associated with high postoperative pain scores and opioid
requirements. Epidural analgesia has been reported to be an effective and safe method to
control postoperative pain after spinal instrumentation surgery, but the overall effects of
pain management on postoperative length of stay and recovery remains debatable.
However, in a multimodal approach, including multimodal non-opioid analgesia to control
postoperative pathophysiology and rehabilitation, complications and hospital stay have been
reduced after arthroscopy, hip arthroplasty and knee arthroplasty, hip fractures and
abdominal surgery and other procedures, when combined with an enhanced recovery program.
The aim of the study is to assess the effect and safety of a combined analgesic regimen
consisting of local anesthetic, intra-operative and post-operative continuous epidural
analgesia and a single dose ketorolac together with a fast track rehabilitation program
after 360 degree lumbar fusion for degenerative disc disease and spondylolisthesis < 2
;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject)
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT05114135 -
TLIF Osteo3 ZP Putty Study (Also Known as the TOP Fusion Study)
|
N/A | |
Recruiting |
NCT04378543 -
Safety Evaluation of ART352-L in Subjects Undergoing Posterolateral Spinal Fusion
|
Phase 1/Phase 2 | |
Withdrawn |
NCT03223701 -
Efficacy of Using Solum IV and BMC With GFC in TLIF
|
Phase 4 | |
Not yet recruiting |
NCT06000319 -
Natural Matrix Protein™ (NMP™) Fibers in Cervical and Lumbar Interbody Fusion
|
||
Completed |
NCT00996073 -
Safety and Preliminary Efficacy Study of NeoFuse in Subjects Requiring Lumbar Interbody Fusion
|
Phase 2 | |
Recruiting |
NCT05538416 -
Short-term Clinical Outcome of Cortical Bone Trajectory Compared With the Traditional "Open" and Minimal Invasive Posterior Lumbar Interbody Fusion
|
||
Withdrawn |
NCT02530775 -
"Is Instrumentation Necessary for "Static" Degenerative Spondylolisthesis"
|
N/A | |
Terminated |
NCT03570801 -
SLIP II Registry: Spinal Laminectomy Versus Instrumented Pedicle Screw Fusion
|
N/A | |
Enrolling by invitation |
NCT04418830 -
Lumbar Interbody Implant Study
|
||
Completed |
NCT03303300 -
The Five-repetition Sit-to-stand Test for Lower Back Pain or Radiculopathy
|
N/A | |
Withdrawn |
NCT00810212 -
Safety and Efficacy Study of NeoFuse in Subjects Requiring Posterolateral Lumbar Fusion
|
Phase 1/Phase 2 | |
Terminated |
NCT04483297 -
First-In-Human Study of AK1320 Encapsulated Microspheres (AK1320 MS)
|
Phase 1 | |
Completed |
NCT03898232 -
Fibergraft Interbody Fusion Retrospective
|
||
Completed |
NCT00726310 -
Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal Instability
|
||
Recruiting |
NCT06154005 -
OsteoAdapt SP Advanced Bone Graft Feasibility Study - Transforaminal Interbody Lumbar Fusion
|
Phase 1/Phase 2 | |
Completed |
NCT04418817 -
Modulus in XLIF Study
|
||
Completed |
NCT02087267 -
Lumbar Fusion With The Icotec CF/PEEK Pedicle System In Combination With The Icotec CF/PEEK TLIF Cage ETurn™
|
||
Terminated |
NCT01528072 -
Dynesys Spinal System Post Market 522 Study
|
N/A | |
Active, not recruiting |
NCT03733626 -
Clinical Outcomes Associated With the Use of ViviGen® for the Treatment of Lumbar Degenerative Disc Disease
|
N/A | |
Active, not recruiting |
NCT05993195 -
Re-operation Rates of Concorde Bullet Device Versus Conduit Titanium Interbody Graft for Lumbar Fusion
|