Spine Fusion

10

Review clinical trials related to Spine Fusion. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

The Effect of Zolpidem on Outcomes Following Lumbar Spine Fusion

The purpose of this study is to evaluate if peri-operative zolpidem for posterior lumbar spinal fusion improves patient reported outcomes following surgery.

Participants needed: 140
Trial details
Phase: Phase 4Age: 18-75Biological sex: AllType: InterventionalSponsor: University of Southern CaliforniaUpdated: May 1, 2026Locations: 1
Eligibility criteria

degenerative lumbar disease [+2]

currently use a sleep aid nightly [+6]

Status: Recruiting

Personalized Perioperative Analgesia Platform (PPAP) for Pediatric Spine Fusion Surgery (sIRB)

The purpose of this collaborative CTSA application is to develop an innovative perioperative precision analgesia platform (PPAP) to improve analgesia and reduce serious immediate and long-term adverse outcomes of perioperative opioids in children undergoing painful surgery.

Participants needed: 300
Trial details
Age: 10-21Biological sex: AllType: InterventionalSponsor: Senthil SadhasivamUpdated: Apr 13, 2026Locations: 5
Eligibility criteria

Children ages 10 to 21 [+4]

Serious illness [+2]

Status: Recruiting

Post Marketing Study of MagnetOs Easypack Putty Standalone Compared to Demineralized Bone Matrix or Fibers Mixed With Autograft in Patients Undergoing Posterolateral Lumbar Fusion

This is a phase IV post-marketing study for MagnetOs Easypack Putty. MagnetOs Easypack Putty is a synthetic bone graft extender product that is routinely used by surgeons as a treatment for patients with degenerative disc disease or spinal trauma undergoing spinal fusion surgery. In this study, MagnetOs Easypack Putty will be used according to the latest U.S. Instructions For Use, standalone in the posterolateral spine.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Kuros Biosurgery AGUpdated: Mar 20, 2026Locations: 6
Eligibility criteria

Patient is able to read/be read, understand, and provide written informed consen... [+8]

Requires > two-level fusion or expected to need secondary intervention within on... [+15]

Status: Recruiting

MagnetOs Flex Matrix Compared to Trinity Elite Mixed With Local Autograft in Patients Undergoing up to Four-level Instrumented Posterolateral Fusion

This is a phase IV post-marketing study for MagnetOs Flex Matrix. MagnetOs Flex Matrix is a synthetic bone graft extender product that is routinely used by surgeons as a treatment for patients with degenerative disc disease and undergoing spinal fusion surgery. In this study, MagnetOs Flex Matrix will be used according to the latest U.S. Instructions For Use, specifically as a bone graft extender mixed with autograft in a 1:1 vol.% in the posterolateral spine. Trinity Elite will also be used according to its latest IFU approved in the US. Specifically, this cellular based allograft is an allograft intended for the treatment of musculoskeletal defects.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Kuros Biosurgery AGUpdated: Feb 25, 2026Locations: 7
Eligibility criteria

Patient is able to read/be read, understand, and provide written informed consen... [+3]

Requires > four-level fusion or expected to need secondary intervention within o... [+15]

Status: Recruiting

Trans-Auricular Stimulation for Postoperative Inflammation in Spine Surgery

This study is a randomized controlled trial that will evaluate the effect of non-invasive auricular vagal nerve stimulation on inflammatory markers, glycemic control, postoperative pain, and inflammation-related clinical outcomes after long-segment spinal fusion surgeries when compared to current accepted management.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Alexander T. YahandaUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Long-segment spinal fusions (defined as constructs spanning at least L2-pelvis f... [+1]

Patients <18 years of age [+6]

Status: Not yet recruiting

Rate of Bone Union After Surgery With Stand-alone Fibergraft

Some people have back problems caused by degenerative conditions or instability of the spine (eg. Spondylolisthesis). These problems can lead to pain, nerve issues, or difficulties in walking. A common treatment is a type of back surgery called lumbar interbody fusion, which helps stabilize the spine. At the St. Maartenskliniek in the Netherlands, doctors have been using a special material called Fibergraft Bioactive Glass Putty for such surgeries since 2023. This material helps bones grow and heal, and it's placed inside the spine without needing extra bone from another part of the body. This study will look at how well this material works by evaluating how many patients' bones successfully healed after surgery using this material. It will also look at how patients feel and recover after the procedure

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: AO Innovation Translation CenterUpdated: Sep 30, 2025Locations: 1
Eligibility criteria

Adults ≥ 18 years old [+8]

Revision surgery [+5]

Status: Recruiting

Effect of Magnesium on Neuromonitoring

Intraoperative neurophysiologic monitoring (IONM) is commonly used during complex spinal surgery to monitor the integrity of neural structures and improve the perioperative safety profile. Transcranial Motor Evoked Potentials (TcMEPs) monitor the integrity of the motor pathways and are one of the most commonly used monitoring modalities in spinal surgery. Because inhaled anesthetics can negatively affect the ability to monitor TcMEPs, anesthesiologists commonly use a combination of propofol and opioids to maintain the anesthetic state. Additionally, anesthesiologists will frequently administer intravenous infusions of medications that can decrease postoperative pain and opioid use (called opioid-sparing adjuncts) because spinal surgeries result in significant postoperative pain. Despite the increasing use of these agents, there is scant clinical data about how they may affect the integrity of TcMEP monitoring. Magnesium (Mg), a N-methyl-d-aspartate receptors (NMDA) receptor antagonist, is one of the adjuncts with robust data supporting clinical efficacy to decrease pain and opioid use on TcMEPs. Mg has been used clinically for decades. The investigators commonly utilize intravenous magnesium as a component of our spinal anesthesia protocol. However, there is only a single case report that discusses the effects of Mg on TcMEPs. Here the investigators propose a prospective clinical trial to quantitatively assess the effects of various Mg plasma levels on TcMEPs. There is a lack of literature on the pharmacokinetics of magnesium in non-pregnant patients.

Participants needed: 20
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: University of California, San FranciscoUpdated: Jul 8, 2025Locations: 1
Eligibility criteria

Patients with a history of significant cardiac disease (LVEF <35%, 2nd/3rd-degre... [+3]

Status: Recruiting

Effect of Ketamine on Intraoperative Motor Evoked Potentials

The goal of this clinical trial is to learn about the effect of ketamine on intraoperative motor evoked potentials in adult patients undergoing thoracolumbar spinal fusions. Participants will undergo a standard anesthetic. In addition to the standard anesthetic, the patients will be administered increasing doses of ketamine with motor-evoked potentials being measured at each dose, to assess any impacts.

Participants needed: 20
Trial details
Phase: Phase 3Age: 18-100Biological sex: AllType: InterventionalSponsor: University of California, San FranciscoUpdated: May 7, 2025Locations: 1
Eligibility criteria

Adult patients (>18 years of age) undergoing posterior spinal fusions.

Sensitivity or allergy to ketamine. [+5]

Status: Not yet recruiting

Spine Surgery Video Observation Study. The Creation of a Benchmark Video (RGB-Depth) Dataset to Investigate the Feasibility of Developing a Markerless Tracking System for Spine Surgery.

The primary study objective is to build a video dataset, consisting of both colour and depth information, of spine surgery that includes both 'open' and 'minimally invasive' (MIS) surgeries. Using accompanying preoperative CT scans of the patient's spine, we aim to develop a markerless tracking system for spine surgery, which the collected dataset will be used to both train, and then benchmark against.

Participants needed: 25
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Imperial College LondonUpdated: Aug 30, 2024
Eligibility criteria

Candidate surgeries include all spine surgeries taking a posterior approach. Thi...

Candidate surgeries will be excluded if the patient is under the age of 18 or th...

Status: Not yet recruiting

Steroids After Spine Fusion Surgery

This trial studies how well low-dose postoperative corticosteroids (FDA approved) affect patient outcomes (patient reported outcomes, pain medication use, length of stay, major complications, and time to first bowel movement) after thoracic and/or lumbar spine fusion surgery.

Participants needed: 420
Trial details
Phase: Phase 4Age: 50+Biological sex: AllType: InterventionalSponsor: Oregon Health and Science UniversityUpdated: Apr 22, 2024Locations: 1
Eligibility criteria

All patients over the age of 50 undergoing thoracic and/or lumbar fusion with a...

Patient is already taking chronic steroids [+3]