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Spinal Surgery Clinical Trials

A listing of Spinal Surgery medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

RESULTS

Found (17) clinical trials

The purpose of the study is to better understand the use of nerve transfer surgery on patients with spinal cord injuries. This study lasts up to 24 months. All study visits are performed at standard of care visits at 6, 12, 18, and 24 months post-operatively. There will be standard ...

Phase N/A

Researchers at the University of Kentucky are inviting you to participate in a noninvasive, painless study that will involve: Recording of brain signals from electrodes on your scalp while you perform a repetitive hand grip task Brief peripheral nerve stimulation (PNS) in response to changes detected in your brain signals ...

Phase N/A

Tranexamic Acid Dosing in Adult Spinal Deformity Surgery

After consent is obtained and the patient is enrolled in the trial, patients will be assigned de-identified, unique identification (ID) numbers. Randomization of these IDs to either low or high dose TXA will occur via a computer generated random assignment. Given the variations that may exist in surgical technique (e.g. ...

Phase

ADDRESS - Adult Deformity Robotic vs. Freehand Surgery to Correct Spinal Deformity

To quantify potential short- and long-term benefits of robotically-guided minimally invasive (MIS) or open-approach spine surgery in adult patients undergoing multi-level spinal instrumentation surgery, in comparison to image- or navigation-guided instrumentation in a matching cohort of control patients, performed using a freehand technique, both in MIS and open approaches.

Phase N/A

A Feasibility Study to Evaluate the TURRIS Facet Fusion System in Lumbar Spinal Surgery

The Turris® Facet Fuser is an investigational resorbable device intended to support spinal segment fusion in individuals suffering from degenerative lumbar spinal diseases. The device is directly inserted in the facet joint of the affected segment using the BoneWelding® technology, a soft tissue sparing, ultrasound based insertion method which confers ...

Phase N/A

dHACM in Lumbar Decompression and Microdiscectomy Surgery

The objective of this prospective study is to evaluate the safety and efficacy of dHACM on clinical outcomes in lumbar laminectomy and microdiscectomy patients randomized to one of two groups: 1) without dHACM (control) or 2) dHACM.

Phase

dHACM in Lumbar Decompression and Microdiscectomy Surgery

The present study investigates the product dHACM, which is unique in that it utilizes an amniotic membrane that has anti-scarring and anti-keloid formation properties. dHACM also contains growth factors that promote healing. The growth factors present in dHACM are Epidermal Growth Factor (EGF), Transforming Growth Factor Beta (TGF-β), Fibroblast Growth ...

Phase N/A

StruCtuRal And FuncTional Brain Alterations by Conventional Spinal Cord Stimulation And High DensitY Stimulation

When patient meets all inclusion criteria and no exclusion criteria, a neuroimaging protocol will be obtained at baseline, prior to trial implantation of SCS. At trial implantation a Vectris® SureScan® MRI 1x8 lead will be implanted, targeted by intraoperative mapping. This lead will be connected to a temporary extension cable ...

Phase N/A

Treatment for Chronic Spinal Cord Injury: Surgery With Rehabilitation vs Rehabilitation

Safety Issues: Safety issues need to be watched are: occurrence of known and unknown undesirable incidences, moving up injury levels, loss of previously preserved neurological functions, vital physical signs, and worsening of EKG and lab results. If unforeseen issues occur, patients will be consulted to determine whether treatments will be ...

Phase N/A

Assessment of the Performance of LYoplant ONlay for Duraplasty

The aim of this Post Market Clinical Follow-up Study is to collect clinical data on the performance of Lyoplant® Onlay. To assess the performance of the product, various safety and efficacy parameters have been selected.

Phase N/A