Spondylolisthesis Clinical Trial
Official title:
Return of Bowel Function After One or Two Level Anterior Lumbar Interbody Fusion With Chewing Gum
Researchers are trying to identify is chewing gum improves bowel function after anterior lumbar interbody fusion
Aims, purpose, or objectives: 1. Observe changes in bowel pattern based on gum-chewing 2. Examine bowel function after anterior lumbar interbody fusion 3. Measure length of time to return of bowel function after anterior lumbar interbody fusion 4. Compare return of bowel function in patients who chew gum and patients standardized to usual post-operative care 5. Measure the hospital length of stay amongst study groups 6. Measure post-operative pain amongst study groups Background (Include relevant experience, gaps in current knowledge, preliminary data, etc.): One or two level anterior lumbar interbody fusions are designed to correct lumbar spondylosis and spondylolisthesis, which can cause debilitating back and leg pain. This surgery involves an anterior approach, which often requires displacement of bowel for the length of the surgery. Patients frequently have a slow return of bowel function secondary to anesthetic time, opioid use, and primarily due to the bowel displacement intraoperatively. Because this is a one or two level surgery, many patients would benefit from same-day discharge but often remain inpatient several days due to slow return of bowel function. Gum chewing has been shown to decrease the time for return to bowel function (RBF) in colorectal and gynecology patients postoperatively. Gum chewing and RBF has been studied in the spine population for posterior operations but not anterior spine surgery. This study aims to identify whether chewing gum has an impact on patient's report of pain, RBF, length of stay, and subjective report of satisfaction post-operatively. This could be an outpatient operation; however, pain and RBF often prevent patients from discharging home the same day of surgery. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT03883022 -
Vancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection for Spine Surgery
|
N/A | |
Active, not recruiting |
NCT04542577 -
PMCF Study on the Safety and Performance of PROSPACE 3D / PROSPACE 3D OBLIQUE / TSPACE 3D
|
||
Recruiting |
NCT04477447 -
PMCF Study on the Safety and Performance of CESPACE 3D
|
||
Completed |
NCT02558621 -
New Robotic Assistance System for Spinal Fusion Surgery
|
N/A | |
Terminated |
NCT01461005 -
A Postmarket Surveillance Study of the Paradigm Spine Dynamic Stabilization System (DSS)
|
N/A | |
Completed |
NCT00405691 -
Safety and Effectiveness Study of the TOPS System, a Total Posterior Arthroplasty Implant Designed to Alleviate Pain Resulting From Moderate to Severe Lumbar Stenosis
|
Phase 3 | |
Completed |
NCT00205101 -
Clinical Outcome Study of the Triad Allograft for Posterior Lumbar Fusion
|
||
Enrolling by invitation |
NCT04204135 -
The Course of Hip Flexion Weakness Following LLIF or ALIF
|
||
Recruiting |
NCT05238740 -
Comparison of Standalone Anterior Lumbar Interbody Fusion (ALIF) L5/S1 Performed With Either rhBMP-2 or ViviGen®
|
N/A | |
Not yet recruiting |
NCT02805985 -
Post-market Surveillance Study of FLXfit™ TLIF Interbody Fusion Device
|
N/A | |
Completed |
NCT02966639 -
Validation of Appropriateness Criteria for the Surgical Treatment of Lumbar Degenerative Spondylolisthesis
|
||
Completed |
NCT02931279 -
PASS OCT® Post-market Clinical Follow-up
|
||
Active, not recruiting |
NCT02057744 -
MIS ReFRESH: Robotic vs. Freehand Minimally Invasive Spinal Surgeries
|
||
Completed |
NCT01711203 -
The Addition of a Pilates Program for Short-Term Improvements in Patients With Spondylolysis or Spondylolisthesis
|
N/A | |
Completed |
NCT00549913 -
Study of 3 Doses of NeoFuse Combined With MasterGraft Granules in Subjects Requiring Posterolateral Lumbar Fusion (PLF)
|
Phase 1/Phase 2 | |
Terminated |
NCT00254852 -
Evaluation of Radiographic and Patient Outcomes Following Lumbar Spine Fusion Using Demineralized Bone Matrix (DBM) Mixed With Autograft
|
N/A | |
Terminated |
NCT00095095 -
Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™ Fusion Device
|
Phase 4 | |
Active, not recruiting |
NCT03956537 -
PMCF Neo Pedicle Screw and Cage Systems
|
||
Recruiting |
NCT05182489 -
Adaptix RCT Evaluating Adaptix™ Versus PEEK Cages
|
N/A | |
Completed |
NCT02884440 -
Transverse Abdominis Plane Block for Anterior Approach Spine Surgery
|
Phase 2 |