Spinal Fusion Clinical Trial
Official title:
Efficacy of ARISTA-AH for Restoring Hemostasis Following Posterior Long-segment Spinal Fusion.
The aim of this study is to assess the efficacy of the ARISTA AH for restoring hemostasis following a long segment posterior spinal fusion.
After being informed about the study and potential risks, all patients giving written inform consent will be included in the study during their preoperative visit. After eligibility criteria checking and based on their respective surgical indication, participants will be randomized in a single-blinded and stratified manner (participant only) in a 1:1 ratio to ARISTA-AH or no ARISTA-AH. The stratification process will consider the number of instrumented vertebra during each surgery (level 1: 5 to 8 vertebra; level 2: 9 or more instrumented vertebra). ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT04037059 -
Impact of Body Habitus (Arm Span and Abdominal Girth) on Activities of Daily Living (ADL)
|
||
| Recruiting |
NCT03883022 -
Vancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection for Spine Surgery
|
N/A | |
| Not yet recruiting |
NCT06003010 -
Yoga for Adolescent Idiopathic Scoliosis (AIS) Patients
|
N/A | |
| Completed |
NCT01136590 -
Multicenter, Randomized Placebo-controlled Clinical Trial to Evaluate the Effect of Perioperative Use of Tranexamic Acid on Transfusion Requirements and Surgical Bleeding in Major Spine Surgery
|
Phase 4 | |
| Completed |
NCT01235650 -
Prevalence of Inadvertent Hyperventilation During Intraoperative Anesthetic Care
|
N/A | |
| Completed |
NCT03459404 -
Sufentanil NanoTab PCA System/15 mcg for Acute Post-Operative Pain in Vertebral Surgery: A Preliminary Investigation
|
||
| Recruiting |
NCT05010148 -
A Clinical Trial of Intravenous Lidocaine After Spinal Surgery to Prevent Delirium and Reduce Pain
|
Phase 3 | |
| Recruiting |
NCT04605120 -
Allogeinic Bone Paste
|
N/A | |
| Completed |
NCT03826329 -
Risk Factors of Second Surgery for Adjacent Segment Disease Following Anterior Cervical Discectomy and Fusion
|
||
| Recruiting |
NCT04601363 -
Personalized Spine Study Group (PSSG) Registry
|
||
| Completed |
NCT00994656 -
Is Pleth Variability Index (PVI) a Surrogate for Pulse Pressure Variations (PPV) in Pediatric Spine Fusion (SF) Surgery?
|
N/A | |
| Completed |
NCT00152152 -
Use of Radiostereometric Analysis Beads (RSA) to Measure Motion in the Spine, Following Lumbar Spinal Surgery
|
N/A | |
| Terminated |
NCT03425799 -
Efficacy and Safety of Tranexamic Acid in Spinal Fusion Surgery
|
Phase 3 | |
| Not yet recruiting |
NCT06368245 -
Durability of Suppl. Rod Constructs-SuppleMentAry Rod Technique for Long-segment Posterior Instrumented Spinal Fusions
|
||
| Withdrawn |
NCT03908203 -
Minimally Invasive Surgery Techniques for One-level Degenerative Lumbar Deformities Correction
|
N/A | |
| Terminated |
NCT03378973 -
The Effects of Dexmedetomidine Dose on Motor Evoked Potentials
|
Phase 4 | |
| Completed |
NCT05936047 -
Bone Marrow Clot for Posterior Lumbar Fusion
|
N/A | |
| Not yet recruiting |
NCT03692845 -
Minimally Invasive Versus Open Transforaminal Lumbar Interbody Fusion
|
N/A | |
| Completed |
NCT00152165 -
Use of Radiostereometric Analysis (RSA) Following Spinal Fusion Versus the DYNESYS Stabilization System
|
N/A | |
| Recruiting |
NCT03644407 -
Galeazzi Spine Surgery RegistryGaleazzi Spine Registry: Prospective Study for Clinical Monitoring
|